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

THERMASSAGE

K Number: K061001 · Decision Oct 12, 2006
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
18
Review Days
184

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Basic Information

Device Name
THERMASSAGE
K Number
K061001
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Thermage, Inc.
Date Received
April 11, 2006
Decision Date
October 12, 2006
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 Thermage, Inc.

K Number Device Name
K101490 FRAXEL RE:STORE DUAL LASER SYSTEM: MODEL, MC-SYS-SR1500-D-US
K072849 MODIFICATION TO THERMAGE THERMACOOL SYSTEM
K052936 THERMAGE THERMACOOL SYSTEM
K053365 MODIFICATION TO THERMAGE THERMACOOL SYSTEM
K052778 THERMAGE THERMACOOL SKIN MARKETING
K051710 THERMAGE THERMACOOL COUPLING FLUID
K043402 THERMAGE THERMACOOL SYSTEM
K040135 THERMAGE THERMACOOL SYSTEM
K033942 THERMAGE THERMACOOL SYSTEM
K032088 MODIFICATION TO THERMACOOL TC SYSTEM
Search all 18 clearances from Thermage, Inc. →