Impact, Models 306/307
FDA 510(k) K820338 · Impact Instrumentation, Inc.
510(k) numberK820338
Submission
- Device name
- Impact, Models 306/307
- Applicant
- Impact Instrumentation, Inc.
Mchenry, IL, US - Received
- February 8, 1982
- Decision date
- March 2, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- BTA – Pump, Portable, Aspiration (Manual Or Powered)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4780
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code BTA
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253629 | Momcozy Nasal Aspirator (BN007)BTA · Traditional | Shenzhen Root Innovation Technology Co., Ltd. | 05/26/2026SE |
| K260134 | Baby Nasal Aspirator (BN006, BN006-A, BN006-B, BN006-C, BN006-D, BN02; BN008, BN008-A…BTA · Traditional | Shenzhen Root Innovation Technology Co., Ltd. | 05/15/2026SE |
| K260892 | Suction Pump (SU-90)BTA · Traditional | Shenzhen HugeMed Medical Technical Development… | 05/14/2026SE |
| K260473 | Electric nasal aspirator (BC027, BC030, BC033, BC035, BC035B)BTA · Traditional | Shenzhen Kingboom Technology Co., Ltd. | 05/12/2026SE |
| K253107 | Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90)BTA · Traditional | Shenzhen Dongjiang Technology Co., Ltd. | 04/14/2026SE |
| K260147 | Electric nasal aspirator (BC026, BC025, BC023, BC028, BC029, BC036)BTA · Traditional | Shenzhen Kingboom Technology Co., Ltd. | 03/13/2026SE |
| K251450 | Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator…BTA · Special | Shenzhen Desida Technology Co., Ltd. | 06/06/2025SE |
| K244033 | Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NASA606,NASA608,NASA610)BTA · Traditional | Shenzhen Desida Technology Co., Ltd. | 05/16/2025SE |
| K251101 | AIRO Suction Unit (AIRO-01)BTA · Traditional | Cro, LLC | 04/26/2025SE |
| K250697 | Electric Nasal Aspirator (BC026, BC025, BC023)BTA · Traditional | Shenzhen Kingboom Technology Co., Ltd. | 04/23/2025SE |
More from Shenzhen Kingboom Technology Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K133196 | Impact Model 323 AspiratorJCX · Traditional | 03/10/2014SE |
| K111473 | Uni-Vent (R) Model 731 Series Portable Critical Care VentilatorCBK · Traditional | 02/16/2012SE |
| K103318 | Uni-Vent 731 Series Model Emv+ Portable Critical Care VentilatorCBK · Traditional | 04/07/2011SE |
| K091238 | UNI-VENT-731 Series Ventilators, Model 731EMV+CBK · Traditional | 08/13/2009SE |
| K071526 | Uni-Vent 731 Series Ventilators, Model 731, 731EMVCBK · Traditional | 12/10/2008SE |
| K051476 | Uni-Vent Model 73XBTL · Traditional | 10/28/2005SE |
| K032386 | Uni-Vent Model 730AEV (Automatic Emergency Ventilator)BTL · Traditional | 03/26/2004SE |
| K022062 | Impact, Universal Single-Limb, Ventilator Circuit, Model 820-0099-00MOD · Abbreviated | 05/06/2003SE |
| K951423 | Aspirator, Continuous & Programmable IntermittentBTA · Traditional | 04/18/1995SE |
| K941096 | Electric Vacum PumpBTA · Traditional | 01/05/1995SE |
Questions and answers
When was Impact, Models 306/307 cleared by the FDA?
Impact, Models 306/307 (K820338) received a 510(k) decision of Substantially Equivalent on March 2, 1982, 22 days after the submission was received.
What is the product code of K820338?
The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.