The following data is part of a premarket notification filed by Sealite Sciences, Inc. with the FDA for Sealite Sciences, Inc. Aqualite Human Growth Hormone Assay.
Device ID | K972761 |
510k Number | K972761 |
Device Name: | SEALITE SCIENCES, INC. AQUALITE HUMAN GROWTH HORMONE ASSAY |
Classification | Radioimmunoassay, Human Growth Hormone |
Applicant | SEALITE SCIENCES, INC. 3000 NORTHWOODS PKWY., #200 Norcross, GA 30071 |
Contact | Cathryn N Cambria |
Correspondent | Cathryn N Cambria SEALITE SCIENCES, INC. 3000 NORTHWOODS PKWY., #200 Norcross, GA 30071 |
Product Code | CFL |
CFR Regulation Number | 862.1370 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-07-24 |
Decision Date | 1997-09-25 |
Summary: | summary |