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

LASER, PHOTOCOAGULATION

K Number: K782065 · Decision Dec 28, 1978
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
32
Review Days
15

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Basic Information

Device Name
LASER, PHOTOCOAGULATION
K Number
K782065
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Cavitron Corp.
Date Received
December 13, 1978
Decision Date
December 28, 1978
Product Code
HQF
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HQF Laser, Ophthalmic

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