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

MFG-05

K Number: K230780 · Decision Oct 5, 2023
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
95
Applicant Total
13
Review Days
197

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Basic Information

Device Name
MFG-05
K Number
K230780
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5320
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer Medizinsysteme GmbH
Date Received
March 22, 2023
Decision Date
October 5, 2023
Product Code
KPI
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KPI Stimulator, Electrical, Non-Implantable, For Incontinence

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Other Clearances by Zimmer Medizinsysteme GmbH

K Number Device Name
K253408 CoolTone
K251378 CoolTone
K240347 PTG-05
K240178 RFG-01
K213256 ThermoTK
K222912 c1Trac
K220601 CoolTone
K220020 Cryo 7
K203488 emField
K192940 CoolTone
Search all 13 clearances from Zimmer Medizinsysteme GmbH →