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

SLIP UROLOGY INTRODUCER SHEATH

K Number: K040520 · Decision May 20, 2004
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
63
Applicant Total
6
Review Days
83

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Basic Information

Device Name
SLIP UROLOGY INTRODUCER SHEATH
K Number
K040520
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Percutaneous Systems, Inc.
Date Received
February 27, 2004
Decision Date
May 20, 2004
Product Code
KNY
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
KNY Accessories, Catheter, G-U

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNY), ordered by most recent decision date.

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Other Clearances by Percutaneous Systems, Inc.

K Number Device Name
K102887 ACCORDION STONE MANAGEMENT DEVICE MODEL AC281205 AND AC3814510
K082803 COAXIAL ACCORDION STONE MANAGEMENT DEVICE, MODEL: COAC12005 - COA20015
K052134 CYSTOGLIDE DILATING INTRODUCER SHEATH
K042877 MICROVERTER URETERAL ACCESS SHEATH
K040519 SLIP UROLOGY CATHETER