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

URETERAL ACCESS SET

K Number: K896385 · Decision Jan 22, 1990
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
13
Review Days
77

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Basic Information

Device Name
URETERAL ACCESS SET
K Number
K896385
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Applied Urology, Inc.
Date Received
November 6, 1989
Decision Date
January 22, 1990
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 Applied Urology, Inc.

K Number Device Name
K921838 ACUCISE URETERAL CUTTING CATHETER
K925282 UROLOGICAL CATHETER AND ACCESSORIES
K920695 URETERAL STENT
K915219 URETHRAL ELECTRODE SHEATH
K912093 DISPOSABLE ASPIRATION IRRIGATION SYSTEM
K920030 SURESEAL ENDOSCOPIC VALVE
K912656 ENDOSCOPIC ELECTRODE
K912903 PERCUTANEOUS RETRACTOR KIT
K905731 FLEXIBLE ENDOSCOPIC ELECTRODE
K903994 URETEROPYELOGRAM CATH FOR RETROGRADE DYE INJECTION
Search all 13 clearances from Applied Urology, Inc. →