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

INTERMITTENT URETHRAL CATHETER TRAY

K Number: K841769 · Decision Aug 24, 1984
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
5
Review Days
116

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
INTERMITTENT URETHRAL CATHETER TRAY
K Number
K841769
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Seamless Hospital Products Co.
Date Received
April 30, 1984
Decision Date
August 24, 1984
Product Code
KOD
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
KOD Catheter, Urological

Similar 510(k) Clearances

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

View all

Other Clearances by Seamless Hospital Products Co.

K Number Device Name
K823061 BRUSH, SCRUB, OPERATING ROOM
K821134 DC PACK TM
K820490 IV START TRAY
K781127 CONNECTING TUBE, CONDUCTIVE, SURG.