FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTER

K Number: K946387 · Decision Mar 30, 1995
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
62
Applicant Total
14
Review Days
125

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Basic Information

Device Name
CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTER
K Number
K946387
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2320
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Capintec, Inc.
Date Received
November 25, 1994
Decision Date
March 30, 1995
Product Code
JJJ
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
JJJ Counter (Beta, Gamma) For Clinical Use

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K071396 CRC 25 SERIES (CRC 25R, CRC 25PET, CRC 25W) DOSE CALIBRATORS
K052595 CRC 15ULTRA
K030175 2 BASIC
K020150 CRC-15BT
K982448 CARDIOLIGHT
K980402 CAPINTEC MODEL 292 ELECTROMETER
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