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

MENTOR SUPER ABSORBENT DRAPE

K Number: K973146 · Decision Dec 4, 1997
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
4
Review Days
104

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Basic Information

Device Name
MENTOR SUPER ABSORBENT DRAPE
K Number
K973146
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mentor Ophthalmics, Inc.
Date Received
August 22, 1997
Decision Date
December 4, 1997
Product Code
KKX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KKX Drape, Surgical, Antimicrobial

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K Number Device Name
K971538 MENTOR GEMINI HEMOSTATIC ERASER
K964312 MENTOR TONO-PEN 3
K960765 MENTOR ADVENT A/B SYSTEM