FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SCANTIBODIES CALCITONIN IMMUNORADIOMETRIC ASSAY (COATED BEAD TECHNOLOGY)

K Number: K961043 · Decision May 6, 1996
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
19
Applicant Total
19
Review Days
53

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Basic Information

Device Name
SCANTIBODIES CALCITONIN IMMUNORADIOMETRIC ASSAY (COATED BEAD TECHNOLOGY)
K Number
K961043
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1140
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Scantibodies Laboratory, Inc.
Date Received
March 14, 1996
Decision Date
May 6, 1996
Product Code
JKR
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JKR Radioimmunoassay, Calcitonin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JKR), ordered by most recent decision date.

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Other Clearances by Scantibodies Laboratory, Inc.

K Number Device Name
K060578 CALCITONIN IMMUNORADIOMETRIC ASSAY (IRMA) (COATED TUBE VERSION)
K060420 MODIFICATION TO WHOLE PTH (1-84) SPECIFIC IMMUNOCHEMILLUMINOMETRIC (ICMA) ASSAY KIT, MODEL 3KG002
K060348 MODIFICATION TO: TOTAL INTACT PTH IMMUNOCHEMILUMINOMETRIC (ICMA) ASSAY KIT
K051888 TOTAL INTACT PTH IMMUNORADIOMETRIC ASSAY (COATED TUBE VERSION), MODEL 3KG013
K051810 WHOLE PTH (1-84) SPECIFIC IMMUNORADIOMETRIC ASSAY (IRMA) COATED TUBE KIT, MODEL 3KG014
K051150 TOTAL INTACT PTH IMMUNOCHEMILUMINOMETRIC (ICMA) ASSAY KIT
K051141 WHOLE PTH (1-84) SPECIFIC IMMUNOCHEMILUMINOMETRIC ASSAY (ICMA), MODEL 3KG002
K050748 ACTH IMMUNORADIOMETRIC (IRMA) ASSAY KIT, MODEL 3KG011
K031534 CYCLASE ACTIVATING PTH (CAP) IMMUNORADIOMETRIC (IRMA) ASSAY KIT, MODEL 3KG001
K021032 ACTH IMMUNORADIOMETRIC (IRMA) DIAGNOSTIC ASSAY KIT, MODEL #3KG100
Search all 19 clearances from Scantibodies Laboratory, Inc. →