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

ERBOKRYO CA CRYOSURGICAL SYSTEM

K Number: K934261 · Decision Apr 26, 1994
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
261
Applicant Total
16
Review Days
238

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Basic Information

Device Name
ERBOKRYO CA CRYOSURGICAL SYSTEM
K Number
K934261
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4350
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Erbe Elektromedizin GmbH
Date Received
August 31, 1993
Decision Date
April 26, 1994
Product Code
GEH
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
GEH Unit, Cryosurgical, Accessories

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K Number Device Name
K261806 ERBECRYO 2 Cryosurgical Unit and Accessories
K253230 ERBECRYO 2 Cryosurgical Unit and Accessories: ERBECRYO 2 cryosurgical unit; Erbe Flexible Cryoprobe
K253915 MOVIVA® Hybrid Ablation Probe
K251108 Erbe ESU Model VIO® 3n with Accessories
K243120 HybridAPC probe
K243451 FiAPC plus probes
K242044 FiAPC plus probes
K240932 HybridTherm System
K232033 HYBRIDknife® flex
K231023 ERBEJET® 2 System
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