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

CRYOCARE CN2 SYSTEM

K Number: K062175 · Decision Aug 28, 2006
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
261
Applicant Total
22
Review Days
28

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Basic Information

Device Name
CRYOCARE CN2 SYSTEM
K Number
K062175
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4350
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Endocare, Inc.
Date Received
July 31, 2006
Decision Date
August 28, 2006
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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Other Clearances by Endocare, Inc.

K Number Device Name
K101333 CRYOCARE CS SURGICAL SYSTEM
K060279 CRYOCARE CS SURGICAL SYSTEM
K050347 MODIFICATION TO CRYOCARE CS SURGICAL SYSTEM
K032333 CRYOCARE CS SURGICAL SYSTEM
K023757 CRYOCARE SURGICAL SYSTEM, MODEL CRYO 20
K021010 MODIFIED CARDIAC CRYOSURGICAL SYSTEM, MODELS 6TCS1 & 6TCSE
K020082 ERECAID CLASSIC SYSTEM; ERECAID ESTEEM MANUAL SYSTEM; ERECAID ESTEEM BATTERY SYSTEM
K011074 CRYOCARE SURGICAL SYSTEM
K003811 CRYOCARE SURGICAL SYSTEM
K011040 CRYOCARE CARDIAC SURGICAL SYSTEM
Search all 22 clearances from Endocare, Inc. →