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

QUANTITOPE 125I-FOLATE RADIOASSAY KIT

K Number: K780508 · Decision May 3, 1978
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
63
Applicant Total
92
Review Days
34

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Basic Information

Device Name
QUANTITOPE 125I-FOLATE RADIOASSAY KIT
K Number
K780508
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1295
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Kallestad Laboratories, Inc.
Date Received
March 30, 1978
Decision Date
May 3, 1978
Product Code
CGN
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
CGN Acid, Folic, Radioimmunoassay

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