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

BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBE

K Number: K873441 · Decision Oct 27, 1987
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
6
Review Days
61

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
BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBE
K Number
K873441
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Bissell Medical Products, Inc.
Date Received
August 27, 1987
Decision Date
October 27, 1987
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 Bissell Medical Products, Inc.

K Number Device Name
K932880 GRASSI GASTROJEJUNOSTOMY TUBE
K914140 GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED
K901683 IMPROVED BAKER TWIN-CUFF SUMP TUBE
K871691 MODIFIED MULTI-LUMEN NASOGASTRIC TUBE
K851672 NYHUS/NELSON TUBE