The following data is part of a premarket notification filed by Clinical Controls, Inc. with the FDA for Hcg/tsh Control- Level 1/level 2/level 3.
Device ID | K935599 |
510k Number | K935599 |
Device Name: | HCG/TSH CONTROL- LEVEL 1/LEVEL 2/LEVEL 3 |
Classification | Multi-analyte Controls, All Kinds (assayed) |
Applicant | CLINICAL CONTROLS, INC. 750 FARROLL RD. SUITE B Grover Beach, CA 93433 |
Contact | James F Godfrey |
Correspondent | James F Godfrey CLINICAL CONTROLS, INC. 750 FARROLL RD. SUITE B Grover Beach, CA 93433 |
Product Code | JJY |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-11-19 |
Decision Date | 1994-10-31 |