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

SMOKE/ODOR EVACUATOR #757

K Number: K912612 · Decision Nov 1, 1991
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
11
Review Days
142

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Basic Information

Device Name
SMOKE/ODOR EVACUATOR #757
K Number
K912612
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
Olsen Electrosurgical, Inc.
Date Received
June 12, 1991
Decision Date
November 1, 1991
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 Olsen Electrosurgical, Inc.

K Number Device Name
K922154 INSULATED SPECULUM W/ SMOKE EVACUATOR OPTION
K912611 OLSEN LAPAROSCOPIC INSTR, DISPOSABLE, SINGLE USE
K913108 TEFLON COATED ELECTRODES/ELECTRODES HANDLES
K885200 600 & 900 SERIES ELECTRODES & 755 & 756 HANDLE
K885199 #500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES
K884171 #875 DISPOSABLE BIOPOLAR CABLE
K884173 #920 DISPOSABLE TUR CABLE
K884174 MODIFIED OLSEN 755/756 SWITCHPENS
K884175 #820/821 BIPOLAR FORCEPS
K884172 MODIFIED OLSEN #770 DISPOSABLE HOLSTER
Search all 11 clearances from Olsen Electrosurgical, Inc. →