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

ROCHE TSH RIA

K Number: K780428 · Decision Mar 30, 1978
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
49
Review Days
13

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Basic Information

Device Name
ROCHE TSH RIA
K Number
K780428
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Hoffmann-La Roche, Inc.
Date Received
March 17, 1978
Decision Date
March 30, 1978
Product Code
JLW
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
JLW Radioimmunoassay, Thyroid-Stimulating Hormone

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Other Clearances by Hoffmann-La Roche, Inc.

K Number Device Name
K850727 BHCG-ROCHE EIA
K831694 RENAK
K830481 ABUSCREEN RADIOIMMUNOASSAY-PHENCYCLIDINE
K830480 ABUSCREEN RADIOIMMUNOASSAY-COCAINE META
K830461 ABUSCREEN RADIOUMMUNOASSAY-METHAQUALONE
K830460 ABUSCREEN RADIOIMMUNOASSAY FOR MORPHINE
K830482 ABUSCREEN RADIOIMMUNOASSAY-AMPHETAMINE
K830462 ABUSCREEN RADIOUMMUNOASSAY--URINE
K830479 ABUSCREEN RADIOIMMUNOASSAY-BARBITURATE
K823579 COBAS REAGENT FOR TOTAL PROTEIN
Search all 49 clearances from Hoffmann-La Roche, Inc. →