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

RUSCH ENTERAL FEEDING TUBE

K Number: K963779 · Decision May 23, 1997
Classifications
1
FEI Numbers
46
Registration Numbers
47
Same Product Code
58
Applicant Total
26
Review Days
245

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
RUSCH ENTERAL FEEDING TUBE
K Number
K963779
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rusch, Inc.
Date Received
September 20, 1996
Decision Date
May 23, 1997
Product Code
FPD
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
FPD Tube, Feeding

Similar 510(k) Clearances

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

View all

Other Clearances by Rusch, Inc.

K Number Device Name
K010420 RUSCH MMG/O'NEIL CATHETER
K993528 RUSCH EMERGENCY MASK
K993194 RUSCH MANUAL RESUSCITATOR BAG
K980870 RUSCH SILICONE FOLEY CATHETER
K974419 RUSCH SIMPLASTIC COUNCILL TIP CATHETER
K970021 RUSCH SUPRAPUBIC TRAY
K963993 RUSCH SIMPLASTIC FOLEY CATHETERIZATION SET
K955564 RUSCH ULTRA TRACHEOFLEX TRACHEOSTOMY SET, CUFFED, STERILE
K955495 RUSCH REINFORCED TRACHAEL TUBE CUFFED, STERILE
K953963 RUSCH SINGLE LUMEN BRONCHIAL TUVBE SET, STERILE, FOR LEFT & RIGHT SIDED BRONCHIAL INTUBATION
Search all 26 clearances from Rusch, Inc. →