The following data is part of a premarket notification filed by Clark Laboratories, Inc. with the FDA for Encore Scl-70.
Device ID | K920150 |
510k Number | K920150 |
Device Name: | ENCORE SCL-70 |
Classification | Antinuclear Antibody, Antigen, 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 | LKJ |
CFR Regulation Number | 866.5100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-01-13 |
Decision Date | 1992-03-18 |