FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

ASEPT PERITONEAL DRAINAGE SYSTEM

K Number: K093796 · Decision Feb 26, 2010
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
14
Applicant Total
20
Review Days
77

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Basic Information

Device Name
ASEPT PERITONEAL DRAINAGE SYSTEM
K Number
K093796
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Pfm Medical, Inc.
Date Received
December 11, 2009
Decision Date
February 26, 2010
Product Code
PNG
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
PNG Peritoneal, Drainage Catheter For Refractory Ascites, Long-Term Indwelling

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Other Clearances by Pfm Medical, Inc.

K Number Device Name
K242763 JetCan® Pro Safety Huber Needle
K241278 ASEPT® Glide Peritoneal Drainage System
K221779 ASEPT Peritoneal Drainage System
K213666 NuCath Wedge Pressure Catheter
K201137 Asept Surgical Face Mask
K192802 primeMidline Catheters
K173114 primeMidline Catheters
K140137 SAFETY BIOPSY NEEDLE SYSTEM
K122402 LPP (LOW PROFILE PORT)
K113354 VETA PERITONEAL DIALYSIS CATHETER
Search all 20 clearances from Pfm Medical, Inc. →