The following data is part of a premarket notification filed by Boots-celltech Diagnostics, Inc. with the FDA for Sucrosep Follicle Stimulating Hormone (fsh) Irma.
Device ID | K862439 |
510k Number | K862439 |
Device Name: | SUCROSEP FOLLICLE STIMULATING HORMONE (FSH) IRMA |
Classification | Radioimmunoassay, Follicle-stimulating Hormone |
Applicant | BOOTS-CELLTECH DIAGNOSTICS, INC. 240 BATH ROAD SLOUGH SL1 4ET Berkshire, England, GB |
Contact | John G Simpson |
Correspondent | John G Simpson BOOTS-CELLTECH DIAGNOSTICS, INC. 240 BATH ROAD SLOUGH SL1 4ET Berkshire, England, GB |
Product Code | CGJ |
CFR Regulation Number | 862.1300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-06-26 |
Decision Date | 1986-08-19 |