FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MICROSURGICAL BLADE

K Number: K812160 · Decision Aug 31, 1981
Classifications
1
FEI Numbers
300
Registration Numbers
300
Same Product Code
47
Applicant Total
10
Review Days
33

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Basic Information

Device Name
MICROSURGICAL BLADE
K Number
K812160
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Vxtra Corp.
Date Received
July 29, 1981
Decision Date
August 31, 1981
Product Code
GES
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GES Blade, Scalpel

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K830385 IRRIGATION/ASPIRATION KIT
K830379 PHAKO KIT
K812620 ADJUSTABLE MICROSURGICAL KNIFE
K812526 MICRO BLADE II
K800557 DISPOSABLE PRE-GELLED ELECTROSURGICAL
K792436 VXTRA BACK PACK EKG ELECTRODE CAT. NO.