The following data is part of a premarket notification filed by Clark Laboratories, Inc. with the FDA for Encore Ss-b.
Device ID | K922340 |
510k Number | K922340 |
Device Name: | ENCORE SS-B |
Classification | Extractable Antinuclear Antibody, Antigen And Control |
Applicant | CLARK LABORATORIES, INC. 53 CEDAR LAKE RD. Blairstown, NJ 07825 |
Contact | Gary Lehnus |
Correspondent | Gary Lehnus CLARK LABORATORIES, INC. 53 CEDAR LAKE RD. Blairstown, NJ 07825 |
Product Code | LLL |
CFR Regulation Number | 866.5100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-05-19 |
Decision Date | 1992-10-16 |