The following data is part of a premarket notification filed by Magnatrade Corp. with the FDA for Scissors, Wire Cutting.
| Device ID | K884095 |
| 510k Number | K884095 |
| Device Name: | SCISSORS, WIRE CUTTING |
| Classification | Scissors, General, Surgical |
| Applicant | MAGNATRADE CORP. 321 S. BOSTON, SUITE 1050 Tulsa, OK 74103 |
| Contact | Marc P Bullock |
| Correspondent | Marc P Bullock MAGNATRADE CORP. 321 S. BOSTON, SUITE 1050 Tulsa, OK 74103 |
| Product Code | LRW |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-28 |
| Decision Date | 1988-10-19 |