The following data is part of a premarket notification filed by Dutchland Laboratories, Inc. with the FDA for Calf (bovine) Serum - Sterile.
Device ID | K812383 |
510k Number | K812383 |
Device Name: | CALF (BOVINE) SERUM - STERILE |
Classification | Sera, Animal And Human |
Applicant | DUTCHLAND LABORATORIES, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | KIS |
CFR Regulation Number | 864.2800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-08-20 |
Decision Date | 1981-09-08 |