Scissor's #'S 2294,2262,2263
FDA 510(k) K791984 · Edward Weck, Inc.
510(k) numberK791984
Submission
- Device name
- Scissor's #'S 2294,2262,2263
- Applicant
- Edward Weck, Inc.
Mchenry, IL, US - Received
- September 25, 1979
- Decision date
- October 17, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FZT – Cutter, Surgical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code FZT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K112400 | SmartshearsFZT · Traditional | Nuscience Consulting and Management Group, LLC | 09/12/2011SE |
| K890818 | Auto Suture Disposable Surgical Trocar*FZT · Traditional | United States Surgical, A Division of Tyco Healthc | 05/04/1989SE |
| K872990 | Micrins Surgical ScissorFZT · Traditional | Micrins Surgical, Inc. | 08/17/1987SE |
| K841741 | Single Hair Transplant GraftFZT · Traditional | Paris Products, Inc. | 07/23/1984SE |
| K841247 | SPC Disposable CutterFZT · Traditional | Surgical Products Corp. | 05/02/1984SE |
| K822448 | Scissors, VariousFZT · Traditional | J. Sklar Mfg. Co., Inc. | 09/14/1982SE |
| K821632 | Surgical Scissors, Set of 3FZT · Traditional | Fred Sammons, Inc. | 06/24/1982SE |
| K821361 | Conphar Tonsil ScissorsFZT · Traditional | Conphar, Inc. | 05/27/1982SE |
| K821355 | Conphar Littauer ScissorsFZT · Traditional | Conphar, Inc. | 05/27/1982SE |
| K821352 | Conphar Iris ScissorsFZT · Traditional | Conphar, Inc. | 05/27/1982SE |
More from Conphar, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K915378 | Weck TrocarHET · Traditional | 06/29/1992SE |
| K914690 | LM15(TM), Catalog Number - 523821GCJ · Traditional | 03/23/1992SE |
| K911915 | Hemoclip IIFZP · Traditional | 01/09/1992SE |
| K914470 | Pneumo-Seal(Tm)GCJ · Traditional | 11/29/1991SE |
| K911272 | Endoscopic Needlholder Cat. Number 114705FHG · Traditional | 07/02/1991SE |
| K902108 | Hem-O-Lok(Tm)FZP · Traditional | 08/06/1990SE |
| K902232 | Weck Electrosurgical Generator #174200GEI · Traditional | 08/02/1990SE |
| K897045 | Bowie-Dick Test Card Catalog Number 008018JOJ · Traditional | 02/15/1990SE |
| K871110 | Coronary Artery Bypass Graft (Cabg) MarkerDSY · Traditional | 08/27/1987SE |
| K851251 | Auto/Manual Titanium Hemoclip Ligating Clip 527200FZP · Traditional | 07/02/1985SE |
Questions and answers
When was Scissor's #'S 2294,2262,2263 cleared by the FDA?
Scissor's #'S 2294,2262,2263 (K791984) received a 510(k) decision of Substantially Equivalent on October 17, 1979, 22 days after the submission was received.
What is the product code of K791984?
The FDA product code is FZT – Cutter, Surgical, a Class I (low risk) device regulated under 21 CFR 878.4800.