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

DAMON D.E.T.E.C.T IMAGE ENHANCER

K Number: K874865 · Decision Dec 23, 1987
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
11
Review Days
26

Basic Information

Device Name
DAMON D.E.T.E.C.T IMAGE ENHANCER
K Number
K874865
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
DAMON CORP.
Date Received
November 27, 1987
Decision Date
December 23, 1987
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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