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

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K Number: K941495 · Decision Jul 15, 1994
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
10
Applicant Total
21
Review Days
109

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Basic Information

Device Name
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K Number
K941495
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4100
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mira, Inc.
Date Received
March 28, 1994
Decision Date
July 15, 1994
Product Code
HQR
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
HQR Apparatus, Cautery, Radiofrequency, Ac-Powered

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Other Clearances by Mira, Inc.

K Number Device Name
K951728 SCHEPENS-YOSHIDA VIDEO BINOCULAR INDIRECT OPHTHALMSCOPE
K950806 SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTS
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
K863246 MIRALITE
K863591 ENDOPHOTOCOAGULATION PROBE
K855105 SIMMONS SHELL
Search all 21 clearances from Mira, Inc. →