FDA 510(k) Substantially Equivalent 🇺🇸 United States

LASER PHOTOCOAGULATOR

K Number: K837306 · Decision Apr 21, 1983
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
23
Review Days
31

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Basic Information

Device Name
LASER PHOTOCOAGULATOR
K Number
K837306
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Hgm, Inc.
Date Received
March 21, 1983
Decision Date
April 21, 1983
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

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