The following data is part of a premarket notification filed by Carwild Corp. with the FDA for Suture Removal Kits Sterile.
Device ID | K833688 |
510k Number | K833688 |
Device Name: | SUTURE REMOVAL KITS STERILE |
Classification | Tape And Bandage, Adhesive |
Applicant | CARWILD CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | KGX |
CFR Regulation Number | 880.5240 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-10-31 |
Decision Date | 1984-05-31 |