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

ENDOCARE PERCUTANEOUS ACCESS SET

K Number: K010339 · Decision Mar 7, 2001
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
22
Review Days
30

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Basic Information

Device Name
ENDOCARE PERCUTANEOUS ACCESS SET
K Number
K010339
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Endocare, Inc.
Date Received
February 5, 2001
Decision Date
March 7, 2001
Product Code
KOD
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
KOD Catheter, Urological

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Other Clearances by Endocare, Inc.

K Number Device Name
K101333 CRYOCARE CS SURGICAL SYSTEM
K062175 CRYOCARE CN2 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
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