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

MAX-E-VAC

K Number: K920217 · Decision Jul 23, 1992
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
10
Review Days
189

Basic Information

Device Name
MAX-E-VAC
K Number
K920217
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
LEISEGANG MEDICAL, INC.
Date Received
January 16, 1992
Decision Date
July 23, 1992
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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