The following data is part of a premarket notification filed by Boots-celltech Diagnostics, Inc. with the FDA for Sucrosep Specific Immunoradiometric Assay.
Device ID | K880758 |
510k Number | K880758 |
Device Name: | SUCROSEP SPECIFIC IMMUNORADIOMETRIC ASSAY |
Classification | Radioimmunoassay, Luteinizing Hormone |
Applicant | BOOTS-CELLTECH DIAGNOSTICS, INC. 240 BATH ROAD SLOUGH SL1 4ET Berkshire, England, GB |
Contact | Stephen R Abbott |
Correspondent | Stephen R Abbott BOOTS-CELLTECH DIAGNOSTICS, INC. 240 BATH ROAD SLOUGH SL1 4ET Berkshire, England, GB |
Product Code | CEP |
CFR Regulation Number | 862.1485 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-02-25 |
Decision Date | 1988-04-18 |