The following data is part of a premarket notification filed by Sclavo, Inc. with the FDA for Uni-fast Creatine Kinase Test (ck).
Device ID | K872029 |
510k Number | K872029 |
Device Name: | UNI-FAST CREATINE KINASE TEST (CK) |
Classification | Differential Rate Kinetic Method, Cpk Or Isoenzymes |
Applicant | SCLAVO, INC. 5 MANSARD COURT Wayne, NJ 07470 |
Contact | King, Ph.d. |
Correspondent | King, Ph.d. SCLAVO, INC. 5 MANSARD COURT Wayne, NJ 07470 |
Product Code | JHS |
CFR Regulation Number | 862.1215 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-05-26 |
Decision Date | 1987-06-17 |