FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

Tranberg CLS Thermal Therapy System

K Number: K142216 · Decision Apr 21, 2015
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
4
Review Days
252

Basic Information

Device Name
Tranberg CLS Thermal Therapy System
K Number
K142216
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clinical Laserthermia Systems AB
Date Received
August 12, 2014
Decision Date
April 21, 2015
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

Similar 510(k) Clearances

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

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Other Clearances by Clinical Laserthermia Systems AB

K Number Device Name
K214125 TRANBERG Thermoguide Therapy System
K163103 Tranberg CLS Diffusor Laser Fiber
K151569 Tranberg CLS Laser Fiber