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

INFRALASE-LASERGUIDE DELIVERY SYSTEM

K Number: K892933 · Decision Jun 22, 1989
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
11
Review Days
62

Basic Information

Device Name
INFRALASE-LASERGUIDE DELIVERY SYSTEM
K Number
K892933
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
XIMED MEDICAL SYSTEMS
Date Received
April 21, 1989
Decision Date
June 22, 1989
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

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K933757 HAND-HELD IRRIGATION PUMP
K933458 SURGICAL TROCARS
K922714 UNIVERSAL IRRIGATION & SUCTION TUBING SET
K922523 BIPOLAR ELECTROSURGICAL PROBES & INSTRUMENTS
K903812 ELECTROPROBE SINGLE-USE SURGICAL PROBE
K900463 LASER DELIVERY SYSTEMS, FIBEROPTICS & CONTACT TIPS
K890775 INFRALASE - LASERGUIDE DELIVERY SYSTEM
K891126 MICROLASE CO2 LASER MICROMANIPULATOR
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