FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

ThermoTK

K Number: K213256 · Decision May 25, 2023
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
77
Applicant Total
13
Review Days
602

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Basic Information

Device Name
ThermoTK
K Number
K213256
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
Zimmer Medizinsysteme GmbH
Date Received
September 30, 2021
Decision Date
May 25, 2023
Product Code
PBX
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
PBX Massager, Vacuum, Radio Frequency Induced Heat

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Other Clearances by Zimmer Medizinsysteme GmbH

K Number Device Name
K253408 CoolTone
K251378 CoolTone
K240347 PTG-05
K240178 RFG-01
K230780 MFG-05
K222912 c1Trac
K220601 CoolTone
K220020 Cryo 7
K203488 emField
K192940 CoolTone
Search all 13 clearances from Zimmer Medizinsysteme GmbH →