Flynn Series III Bag/Mask Unit-
FDA 510(k) K832495 · O-Two Systems Intl., Inc.
510(k) numberK832495
Submission
- Device name
- Flynn Series III Bag/Mask Unit-
- Applicant
- O-Two Systems Intl., Inc.
Walker, MI, US - Received
- July 27, 1983
- Decision date
- September 29, 1983
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- BTM – Ventilator, Emergency, Manual (Resuscitator)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.5915
- Specialty
- Anesthesiology
- Life-sustaining
- Yes
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|---|---|---|---|
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| K243861 | butterflyBVMBTM · Traditional | Compact Medical, Inc. | 04/25/2025SE |
| K221841 | EOlife®BTM · Traditional | Archeon | 03/18/2023SE |
| K212905 | Sotair DeviceBTM · Traditional | Safe Bvm Corporation | 08/18/2022SE |
| K210288 | Disposable Manual ResuscitatorBTM · Traditional | Xiamen Compower Medical Tech. Co., Ltd. | 08/26/2021SE |
| K181583 | Adult Single Use Resuscitator Bag without Pressure Relief, Adult Single Use Resuscitator…BTM · Traditional | Flexicare Medical Limited. | 12/07/2018SE |
| K170663 | Foremount Disposable PVC Resuscitator, Foremount Disposable PEEP Valve, Foremount…BTM · Traditional | Foremount Enterprise Co., Ltd. | 05/11/2018SE |
| K152931 | Ambu SPUR II Adult Resuscitator, Ambu SPUR II Pediatric Resuscitator, Ambu SPUR II…BTM · Abbreviated | Ambu A/S | 08/29/2016SE |
| K132172 | Neonatalie ResuscitatorBTM · Abbreviated | Laerdal Medical A/S | 01/15/2015SE |
| K112852 | Babi Plus Neonatal Resuscitation BagBTM · Traditional | A Plus Medical | 01/13/2012SE |
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| K983857 | Autovent 1500BTL · Special | 11/04/1998SE |
| K983785 | Autovent 1000BTL · Special | 10/29/1998SE |
| K983705 | Emt ResuscitatorBTL · Special | 10/29/1998SE |
| K983643 | Genesis BLSBTL · Special | 10/29/1998SE |
| K960995 | CPR Bio-Barrier FacesheildCBP · Traditional | 01/07/1997SE |
| K940712 | PPM IIICBP · Traditional | 11/14/1994SE |
| K940927 | Rescue BreatherCBP · Traditional | 10/14/1994SE |
| K932170 | Flynnr Genesis II A/C, A/O and IdlhBTL · Traditional | 10/25/1993SE |
| K922810 | OdysseyBTM · Traditional | 01/22/1993SE |
Questions and answers
When was Flynn Series III Bag/Mask Unit- cleared by the FDA?
Flynn Series III Bag/Mask Unit- (K832495) received a 510(k) decision of Substantially Equivalent on September 29, 1983, 64 days after the submission was received.
What is the product code of K832495?
The FDA product code is BTM – Ventilator, Emergency, Manual (Resuscitator), a Class II (moderate risk) device regulated under 21 CFR 868.5915.