The following data is part of a premarket notification filed by V. Mueller O.v. Baxter Healthcare Corp. with the FDA for Flexible Cutting Scissors.
Device ID | K760715 |
510k Number | K760715 |
Device Name: | FLEXIBLE CUTTING SCISSORS |
Classification | Surgical Instruments, G-u, Manual (and Accessories) |
Applicant | V. MUELLER O.V. BAXTER HEALTHCARE CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KOA |
CFR Regulation Number | 876.4730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1976-09-25 |
Decision Date | 1976-10-21 |