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

LIGHT SOURCE, ENDOSCOP, XENON ARC

K Number: K890448 · Decision May 8, 1989
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
25
Applicant Total
21
Review Days
101

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Basic Information

Device Name
LIGHT SOURCE, ENDOSCOP, XENON ARC
K Number
K890448
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Mira, Inc.
Date Received
January 27, 1989
Decision Date
May 8, 1989
Product Code
FFS
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FFS Image, Illumination, Fiberoptic, For Endoscope

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Other Clearances by Mira, Inc.

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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
K863246 MIRALITE
K863591 ENDOPHOTOCOAGULATION PROBE
K855105 SIMMONS SHELL
Search all 21 clearances from Mira, Inc. →