The following data is part of a premarket notification filed by Sealite Sciences, Inc. with the FDA for Aqualite Fsh.
Device ID | K943437 |
510k Number | K943437 |
Device Name: | AQUALITE FSH |
Classification | Radioimmunoassay, Follicle-stimulating Hormone |
Applicant | SEALITE SCIENCES, INC. 187 BEN BURTON CIRCLE Bogart, GA 30622 |
Contact | David F Smith |
Correspondent | David F Smith SEALITE SCIENCES, INC. 187 BEN BURTON CIRCLE Bogart, GA 30622 |
Product Code | CGJ |
CFR Regulation Number | 862.1300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-07-18 |
Decision Date | 1994-12-28 |