Rigid Suction Tips & Related Items
FDA 510(k) K822010 · Kelleher Corp.
510(k) numberK822010
Submission
- Device name
- Rigid Suction Tips & Related Items
- Applicant
- Kelleher Corp.
Mchenry, IL, US - Received
- July 8, 1982
- Decision date
- August 12, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JZF – Tube, Ear Suction
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4420
- Specialty
- Ear, Nose, Throat
Other 510(k)s with product code JZF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K973587 | Exmoor Tympanocentesis Kit (TK/1)JZF · Traditional | Exmoor Plastics , Ltd. | 01/23/1998SE |
| K862903 | Middle Ear Viewer and Fluid CollectorJZF · Traditional | Steven K. Juhn | 11/24/1986SE |
| K853589 | Shah Self-Clearing Mastoid Suction TubeJZF · Traditional | Downs Surgical , Ltd. | 12/23/1985SE |
| K841357 | Micro Fluid ApplicatorJZF · Traditional | Treace Medical, Inc. | 08/24/1984SE |
More from Treace Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K822618 | Emergency Tracheostomy Instrument SetLJW · Traditional | 01/28/1983SE |
| K822268 | Nagashima Ns-Iii ElectronystagmographGWN · Traditional | 01/28/1983SE |
| K823083 | Electrosurgical UnitGEI · Traditional | 12/07/1982SE |
| K823111 | Nystymograph AccessGNN · Traditional | 11/22/1982SE |
| K822252 | ENT Treatment UnitsETF · Traditional | 11/22/1982SE |
| K822272 | Head Mirrors W/Head Lamps & Head BandsHPQ · Traditional | 11/10/1982SE |
| K822017 | Tympanostomy Tubes & Various TypesETD · Traditional | 10/27/1982SE |
| K822257 | Various Types of Light Source HandlesEOQ · Traditional | 10/26/1982SE |
| K822259 | Laryngeal SpatulasEQH · Traditional | 10/22/1982SE |
| K822004 | Face ShieldsKNT · Traditional | 10/20/1982SE |
Questions and answers
When was Rigid Suction Tips & Related Items cleared by the FDA?
Rigid Suction Tips & Related Items (K822010) received a 510(k) decision of Substantially Equivalent on August 12, 1982, 35 days after the submission was received.
What is the product code of K822010?
The FDA product code is JZF – Tube, Ear Suction, a Class I (low risk) device regulated under 21 CFR 874.4420.