The following data is part of a premarket notification filed by Xomed, Inc. with the FDA for Surgical Scissors.
Device ID | K791124 |
510k Number | K791124 |
Device Name: | SURGICAL SCISSORS |
Classification | Scissors, Nasal |
Applicant | XOMED, INC. 1318 LONEDELL RD. Arnold, MO 63010 |
Product Code | KBD |
CFR Regulation Number | 874.4420 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-06-15 |
Decision Date | 1979-06-27 |