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

OPHTHALMIC LASER PHOTOCOAGULATOR

K Number: K853890 · Decision Nov 12, 1985
Classifications
1
FEI Numbers
61
Registration Numbers
62
Same Product Code
176
Applicant Total
21
Review Days
54

Basic Information

Device Name
OPHTHALMIC LASER PHOTOCOAGULATOR
K Number
K853890
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
MIRA, INC.
Date Received
September 19, 1985
Decision Date
November 12, 1985
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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