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

GAMMA COUNTER

K Number: K780344 · Decision Apr 12, 1978
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
62
Applicant Total
52
Review Days
42

Basic Information

Device Name
GAMMA COUNTER
K Number
K780344
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2320
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
LKB INSTRUMENTS, INC.
Date Received
March 1, 1978
Decision Date
April 12, 1978
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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