Conphar Velcro Touniguer
FDA 510(k) K803142 · Conphar, Inc.
510(k) numberK803142
Submission
- Device name
- Conphar Velcro Touniguer
- Applicant
- Conphar, Inc.
Mchenry, IL, US - Received
- December 12, 1980
- Decision date
- January 13, 1981
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- GAX – Tourniquet, Nonpneumatic
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.5900
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code GAX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K931198 | UniquetGAX · Traditional | Icat Systems | 09/01/1993SE |
| K881398 | TourniquetGAX · Traditional | Barretta Products, Research and Development, Inc. | 04/29/1988SE |
| K881176 | Sterile Esmarch BandageGAX · Traditional | Spectrum/Hydro-Med Products, Inc. | 04/11/1988SE |
| K875092 | Degania Silicone TourniquetGAX · Traditional | Degania Silicone , Ltd. | 01/07/1988SE |
| K873928 | Universal TourniquetGAX · Traditional | Dryden Corp. | 10/23/1987SE |
| K872003 | KinderwrapGAX · Traditional | The Kinder Co. | 06/23/1987SE |
| K864897 | Dale Venipuncture Tourniquet, Product No. 1335GAX · Traditional | Dale Medical Products, Inc. | 01/12/1987SE |
| K853472 | Finger TourniquetteGAX · Traditional | Joseph B. Marogil | 10/10/1985SE |
| K853537 | Velcro TourniquetGAX · Traditional | Cp Medical | 09/12/1985SE |
| K852277 | Catapress TourniguetGAX · Traditional | Boehringer Ingelheim Pharmaceuticals, Inc. | 06/27/1985SE |
More from Boehringer Ingelheim Pharmaceuticals, Inc.
| 510(k) | Device | Decision |
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| K821825 | Conphar Silicone Feeding TubeKNT · Traditional | 08/10/1982SE |
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| K821295 | Olsen Hegar Needle HoldersGDF · Traditional | 06/03/1982SE |
| K821289 | Mayo-Hegar Needle HolderGDF · Traditional | 06/03/1982SE |
| K821298 | Backhaus Clamp, 3 1/2HTD · Traditional | 05/28/1982SE |
| K821294 | Tonsil Scissors Straight 5 1/2EGN · Traditional | 05/28/1982SE |
| K821293 | Backhaus Clamp, 5 1/4HTD · Traditional | 05/28/1982SE |
| K821292 | Tonsil Scissors 7EGN · Traditional | 05/28/1982SE |
| K821290 | Littauer Scissors 5 1/2HNF · Traditional | 05/28/1982SE |
| K821286 | Iris Scissors Straight 4 1/2HNF · Traditional | 05/28/1982SE |
Questions and answers
When was Conphar Velcro Touniguer cleared by the FDA?
Conphar Velcro Touniguer (K803142) received a 510(k) decision of Substantially Equivalent on January 13, 1981, 32 days after the submission was received.
What is the product code of K803142?
The FDA product code is GAX – Tourniquet, Nonpneumatic, a Class I (low risk) device regulated under 21 CFR 878.5900.