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

UNICAM I

K Number: K770531 · Decision Apr 5, 1977
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
69
Review Days
15

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Basic Information

Device Name
UNICAM I
K Number
K770531
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1100
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Union Carbide Corp.
Date Received
March 21, 1977
Decision Date
April 5, 1977
Product Code
IYX
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IYX Camera, Scintillation (Gamma)

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