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

DIGAPHOT PHOTOTHERAPY METER MODEL PT 145

K Number: K780162 · Decision Mar 27, 1978
Classifications
1
FEI Numbers
93
Registration Numbers
93
Same Product Code
25
Applicant Total
32
Review Days
55

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Basic Information

Device Name
DIGAPHOT PHOTOTHERAPY METER MODEL PT 145
K Number
K780162
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cavitron Corp.
Date Received
January 31, 1978
Decision Date
March 27, 1978
Product Code
FTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FTA Light, Surgical, Accessories

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