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

UROLOGICAL CATHETERS

K Number: K810281 · Decision Feb 25, 1981
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
14
Review Days
23

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
UROLOGICAL CATHETERS
K Number
K810281
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Latex Ind., Inc.
Date Received
February 2, 1981
Decision Date
February 25, 1981
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 Latex Ind., Inc.

K Number Device Name
K812058 AKRON URINARY DRAINAGE BAT
K791674 BLADDER RETENTION CATHETERIZATION TRAY
K781751 CATHETER, AKRON FOLEY TEFLON
K781433 AKRON MALE EXTERNAL CATHETER
K772277 BLADDER RETENTION-CATHETHERIZATIONTRAY
K780267 CATH TRAY W/OUT CATHETER
K772342 ROBINSON KIT - 750014 & 750016
K772340 CATHETERIZATION KIT 732016-732018
K780268 BLADDER CATH KIT W/OUT CATHETER
K772341 BLADDER KIT - 734000
Search all 14 clearances from Latex Ind., Inc. →