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

BEI MEDICAL SYSTEMS' SMOKE EVACUATOR

K Number: K940266 · Decision Mar 24, 1994
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
4
Review Days
62

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Basic Information

Device Name
BEI MEDICAL SYSTEMS' SMOKE EVACUATOR
K Number
K940266
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5070
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bei Medical Systems Co., Inc.
Date Received
January 21, 1994
Decision Date
March 24, 1994
Product Code
FYD
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
FYD Apparatus, Exhaust, Surgical

Similar 510(k) Clearances

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Other Clearances by Bei Medical Systems Co., Inc.

K Number Device Name
K971492 AUTOMATIC ELECTRONIC HYSTEROSCOPIC INSUFFLATOR
K950663 BEI MEDICAL SYSTEMS MG-1000HS MONOPOLAR GENERATOR
K934286 HYSTEROSCOPE