Mayo Scissor Straight 5 1/2
FDA 510(k) K821275 · Conphar, Inc.
510(k) numberK821275
Submission
- Device name
- Mayo Scissor Straight 5 1/2
- Applicant
- Conphar, Inc.
Walker, MI, US - Received
- May 3, 1982
- Decision date
- May 28, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Other 510(k)s with product code EGN
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K932675 | GXP Dental X-Ray ProcessorEGN · Traditional | Gendex Corp. | 07/26/1993SE |
| K851720 | 1155/1 to 1162/12 Various Types Gum ScissorsEGN · Traditional | Artiberia | 07/02/1985SE |
| K821294 | Tonsil Scissors Straight 5 1/2EGN · Traditional | Conphar, Inc. | 05/28/1982SE |
| K821292 | Tonsil Scissors 7EGN · Traditional | Conphar, Inc. | 05/28/1982SE |
| K821276 | Mayo Scissor Curyed 5 1/2EGN · Traditional | Conphar, Inc. | 05/28/1982SE |
| K821077 | ConpharEGN · Traditional | Conphar, Inc. | 05/24/1982SE |
More from Conphar, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K821825 | Conphar Silicone Feeding TubeKNT · Traditional | 08/10/1982SE |
| K821354 | Conphar Mayo Hegar Needle HolderGDF · Traditional | 06/03/1982SE |
| 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 Mayo Scissor Straight 5 1/2 cleared by the FDA?
Mayo Scissor Straight 5 1/2 (K821275) received a 510(k) decision of Substantially Equivalent on May 28, 1982, 25 days after the submission was received.
What is the product code of K821275?
The FDA product code is EGN – Scissors, Surgical Tissue, Dental, a Class I (low risk) device regulated under 21 CFR 872.4565.