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

TUBING ORGANIZER

K Number: K895706 · Decision Oct 31, 1989
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
1
Review Days
36

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
TUBING ORGANIZER
K Number
K895706
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
3t Products, Inc.
Date Received
September 25, 1989
Decision Date
October 31, 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