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

ThermoPro

K Number: K161862 · Decision Nov 14, 2016
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
44
Applicant Total
13
Review Days
131

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
ThermoPro
K Number
K161862
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5290
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer Medizinsysteme GmbH
Date Received
July 6, 2016
Decision Date
November 14, 2016
Product Code
IMJ
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IMJ Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

Similar 510(k) Clearances

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

View all

Other Clearances by Zimmer Medizinsysteme GmbH

K Number Device Name
K253408 CoolTone
K251378 CoolTone
K240347 PTG-05
K240178 RFG-01
K230780 MFG-05
K213256 ThermoTK
K222912 c1Trac
K220601 CoolTone
K220020 Cryo 7
K203488 emField
Search all 13 clearances from Zimmer Medizinsysteme GmbH →