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

VENTREX COATED TUBE INTACT PTH

K Number: K913434 · Decision Oct 25, 1991
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
85
Applicant Total
82
Review Days
85

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Basic Information

Device Name
VENTREX COATED TUBE INTACT PTH
K Number
K913434
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1545
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ventrex Laboratories, Inc.
Date Received
August 1, 1991
Decision Date
October 25, 1991
Product Code
CEW
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
CEW Radioimmunoassay, Parathyroid Hormone

Similar 510(k) Clearances

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

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Other Clearances by Ventrex Laboratories, Inc.

K Number Device Name
K914554 SPECIFIC IGE EIA-TURBO ASSAY
K913833 VENTREX ALLERGEN DISC
K905612 VENTREX COATED TUBE IGE RADIOIMMUNOASSAY
K905636 VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY
K905247 SHBG IRMA KIT
K904330 TURBO-RAST SPECIFIC IGE ASSAY
K903000 TURBO-RAST SPECIFIC IGE ASSAY
K897083 VENTRESIGN STREP A TEST
K895648 COATED TUBE HIGH SENSITIVITY TSH 100 UIU/ML STAN.
K895649 COATED TUBE HIGH SENSITIVITY TSH 200 UIU/ML STAN.
Search all 82 clearances from Ventrex Laboratories, Inc. →