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

BISTAT ELECTROSURGICAL UNIT 60-5400-001

K Number: K896838 · Decision Feb 13, 1990
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
55
Review Days
70

Basic Information

Device Name
BISTAT ELECTROSURGICAL UNIT 60-5400-001
K Number
K896838
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
ASPEN LABORATORIES, INC.
Date Received
December 5, 1989
Decision Date
February 13, 1990
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

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