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

MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTAT

K Number: K903878 · Decision Nov 5, 1990
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
2
Applicant Total
18
Review Days
75

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Basic Information

Device Name
MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTAT
K Number
K903878
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4100
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Mentor O & O, Inc.
Date Received
August 22, 1990
Decision Date
November 5, 1990
Product Code
HQQ
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
HQQ Apparatus, Cautery, Radiofrequency, Battery-Powered

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Other Clearances by Mentor O & O, Inc.

K Number Device Name
K955245 MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEM
K934320 MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH EXTRUSION ASPIRATION
K912904 MENTOR ODYSSEY PHACOEMULSIFICATION SYSTEM
K915340 MENTOR HORIZON LOW VISION MAGNIFIER
K910637 MENTOR(R) SUR-E-TROL(R)
K911160 MENTOR(R) WET-FIELD(R) II AC COAGULATOR, 22-1305
K895010 MENTOR SPECTACLE BINOCULAR INDIRECT OPHTHALMOSCOPE
K890622 SURG-E-TROL SYSTEM I AND SYSTEM II
K890595 MENTOR ANTERIOR SEGMENT VITRECTOR
K881001 MENTOR WET-FIELD*II COAGULATOR
Search all 18 clearances from Mentor O & O, Inc. →