The following data is part of a premarket notification filed by Theratest Laboratories, Inc. with the FDA for Theratest Lab, Inc., El-anascr Kit.
Device ID | K954106 |
510k Number | K954106 |
Device Name: | THERATEST LAB, INC., EL-ANASCR KIT |
Classification | Antinuclear Antibody (enzyme-labeled), Antigen, Controls |
Applicant | THERATEST LABORATORIES, INC. 2201 WEST CAMPBELL PARK DR. Chicago, IL 60612 -3501 |
Contact | Marius Teodorescu |
Correspondent | Marius Teodorescu THERATEST LABORATORIES, INC. 2201 WEST CAMPBELL PARK DR. Chicago, IL 60612 -3501 |
Product Code | LJM |
CFR Regulation Number | 866.5100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-08-01 |
Decision Date | 1995-11-14 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00854473003057 | K954106 | 000 |
00854473003002 | K954106 | 000 |