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

MIRALITE

K Number: K863246 · Decision Oct 31, 1986
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
21
Review Days
70

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Basic Information

Device Name
MIRALITE
K Number
K863246
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Mira, Inc.
Date Received
August 22, 1986
Decision Date
October 31, 1986
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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K941495 RETURN PATH DIATHERMY HANDLE
K933527 MODIFICATION OF ANTERIOR SEGMENT ELECTRODES
K923629 OPHTHALMIC TRICHIASIS PROBE
K894248 CONVERTER SYSTEM
K891601 POWER OPERATED AND CONTROLLED VITREOUS SCISSORS
K890448 LIGHT SOURCE, ENDOSCOP, XENON ARC
K863591 ENDOPHOTOCOAGULATION PROBE
K855105 SIMMONS SHELL
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