The following data is part of a premarket notification filed by Micromedic Systems with the FDA for Autopak Tsh Monoclonal Irma Kit.
Device ID | K870245 |
510k Number | K870245 |
Device Name: | AUTOPAK TSH MONOCLONAL IRMA KIT |
Classification | Radioimmunoassay, Thyroid-stimulating Hormone |
Applicant | MICROMEDIC SYSTEMS 102 WITMER RD. Horsham, PA 19044 |
Contact | Deborah Lindemuth |
Correspondent | Deborah Lindemuth MICROMEDIC SYSTEMS 102 WITMER RD. Horsham, PA 19044 |
Product Code | JLW |
CFR Regulation Number | 862.1690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-01-21 |
Decision Date | 1987-04-01 |