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

600 & 900 SERIES ELECTRODES & 755 & 756 HANDLE

K Number: K885200 · Decision Jan 13, 1989
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
11
Review Days
28

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Basic Information

Device Name
600 & 900 SERIES ELECTRODES & 755 & 756 HANDLE
K Number
K885200
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Olsen Electrosurgical, Inc.
Date Received
December 16, 1988
Decision Date
January 13, 1989
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEI), 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
K912612 SMOKE/ODOR EVACUATOR #757
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. →