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

ENVIROMATE(TM) SMOKE EVACUATION SYSTEM

K Number: K922555 · Decision Jan 6, 1993
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
3
Review Days
222

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Basic Information

Device Name
ENVIROMATE(TM) SMOKE EVACUATION SYSTEM
K Number
K922555
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
Lase, Inc.
Date Received
May 29, 1992
Decision Date
January 6, 1993
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

Other 510(k) clearances with the same product code (FYD), ordered by most recent decision date.

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Other Clearances by Lase, Inc.

K Number Device Name
K874157 LASE EVACUATOR/ASPIRATOR
K871334 LASE SYSTEM II