The following data is part of a premarket notification filed by Scantibodies Laboratory, Inc. with the FDA for Whole Pth (1-84) Specific Immunoradiometric Assay (irma) Coated Tube Kit, Model 3kg014.
Device ID | K051810 |
510k Number | K051810 |
Device Name: | WHOLE PTH (1-84) SPECIFIC IMMUNORADIOMETRIC ASSAY (IRMA) COATED TUBE KIT, MODEL 3KG014 |
Classification | Radioimmunoassay, Parathyroid Hormone |
Applicant | SCANTIBODIES LABORATORY, INC. 9336 ABRAHAM WAY Santee, CA 92071 |
Contact | Michael Nordstrom |
Correspondent | Michael Nordstrom SCANTIBODIES LABORATORY, INC. 9336 ABRAHAM WAY Santee, CA 92071 |
Product Code | CEW |
CFR Regulation Number | 862.1545 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-07-05 |
Decision Date | 2005-09-09 |