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

BARD MOSS(R) GASTROSTOMY TUBE

K Number: K890871 · Decision Apr 27, 1989
Classifications
1
FEI Numbers
242
Registration Numbers
243
Same Product Code
648
Applicant Total
566
Review Days
65

Basic Information

Device Name
BARD MOSS(R) GASTROSTOMY TUBE
K Number
K890871
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
C.R. BARD, INC.
Date Received
February 21, 1989
Decision Date
April 27, 1989
Product Code
KNT
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
KNT Tubes, Gastrointestinal (And Accessories)

Similar 510(k) Clearances

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

View all

Other Clearances by C.R. BARD, INC.

K Number Device Name
K163001 PowerFlow Apheresis I.V. Port
K162769 Pinpoint GT Introducer Needle
K162443 PowerPICC Provena Catheters
K162377 PowerGlide Pro Midline Catheter
K153280 PowerGlide Pro Midline Catheter
K153359 BardPort®, SlimPort®, and X-Port® Implanted Ports
K153236 Small PerFix Light Plug with 6 x 13.5 cm HydroLight onlay, Medium PerFix Light Plug with 6 x 13.5 cm HydroLight onlay, Large PerFix Light Plug with 6 x 13.5 cm HydroLight onlay, Extra Large PerFix Light Plug with 6 x 13.5 cm HydroLight onlay
K160866 Denali Filter System - Femoral Delivery Kit, Denali Filter System - Jugular/Subclavian Delivery Kit
K141531 POWER-TRIALYSIS SLIM-CATH SHORT-TERM DIALYSIS CATHETER
K150345 Magic3 Go Intermittent Urinary Catheter
Search all 566 clearances from C.R. BARD, INC. →