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

PANDA NEEDLE CATHETER JEJUNOSTOMY KIT

K Number: K921127 · Decision Jan 4, 1993
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
5
Review Days
300

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
PANDA NEEDLE CATHETER JEJUNOSTOMY KIT
K Number
K921127
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Statement
Applicant
Knight Medical, Inc.
Date Received
March 10, 1992
Decision Date
January 4, 1993
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 Knight Medical, Inc.

K Number Device Name
K903086 TUBE GASTROSTOMY
K883848 KMI OXY-BAN
K883886 DOUBLE CLOSED URINARY DRAINAGE SYSTEM
K862489 ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE