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

CLASP RIA KIT, HTSH

K Number: K770915 · Decision Jun 14, 1977
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
32
Review Days
26

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Basic Information

Device Name
CLASP RIA KIT, HTSH
K Number
K770915
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
E. R. Squibb & Sons, Inc.
Date Received
May 19, 1977
Decision Date
June 14, 1977
Product Code
JLW
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
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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K820341 CORTISOL-SQUIBB RADIOIMMUNOASSAY KIT
K811240 SUR-FIT LOOP OSTOMY O.R. SET
K811239 SUR-FIT DISPOSABLE CONVEX INSERT
K811160 SUR-FIT IRRIGATION SLEEVE
K811163 SUR-FIT DISPOSABLE FANGE CAP
K810966 DIAGOXIN SQUIBB RADIOIMMUNOASSAY KIT
K810211 T3 RIA KIT
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