The following data is part of a premarket notification filed by Micromedic Systems with the FDA for Micromedic Combostat Lh/fsh Kit.
Device ID | K872309 |
510k Number | K872309 |
Device Name: | MICROMEDIC COMBOSTAT LH/FSH KIT |
Classification | Radioimmunoassay, Follicle-stimulating Hormone |
Applicant | MICROMEDIC SYSTEMS 102 WITMER RD. Horsham, PA 19044 |
Contact | Deborah L Lindemuth |
Correspondent | Deborah L Lindemuth MICROMEDIC SYSTEMS 102 WITMER RD. Horsham, PA 19044 |
Product Code | CGJ |
CFR Regulation Number | 862.1300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-06-16 |
Decision Date | 1987-07-31 |