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

ELECTROPROBE SINGLE-USE SURGICAL PROBE

K Number: K903812 · Decision Sep 20, 1990
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
11
Review Days
31

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ELECTROPROBE SINGLE-USE SURGICAL PROBE
K Number
K903812
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Ximed Medical Systems
Date Received
August 20, 1990
Decision Date
September 20, 1990
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.

View all

Other Clearances by Ximed Medical Systems

K Number Device Name
K943014 BALLOON ELECTROSURGICAL PROBES AND DEVICES
K946377 ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES
K933757 HAND-HELD IRRIGATION PUMP
K933458 SURGICAL TROCARS
K922714 UNIVERSAL IRRIGATION & SUCTION TUBING SET
K922523 BIPOLAR ELECTROSURGICAL PROBES & INSTRUMENTS
K900463 LASER DELIVERY SYSTEMS, FIBEROPTICS & CONTACT TIPS
K892933 INFRALASE-LASERGUIDE DELIVERY SYSTEM
K890775 INFRALASE - LASERGUIDE DELIVERY SYSTEM
K891126 MICROLASE CO2 LASER MICROMANIPULATOR
Search all 11 clearances from Ximed Medical Systems →