FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CATH TRAY W/OUT CATHETER

K Number: K780267 · Decision Feb 24, 1978
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
13
Applicant Total
14
Review Days
7

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
CATH TRAY W/OUT CATHETER
K Number
K780267
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Latex Ind., Inc.
Date Received
February 17, 1978
Decision Date
February 24, 1978
Product Code
EYZ
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
EYZ System, Urine Drainage, Closed, For Nonindwelling Catheter, Sterile

Similar 510(k) Clearances

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

View all

Other Clearances by Latex Ind., Inc.

K Number Device Name
K812058 AKRON URINARY DRAINAGE BAT
K810281 UROLOGICAL CATHETERS
K791674 BLADDER RETENTION CATHETERIZATION TRAY
K781751 CATHETER, AKRON FOLEY TEFLON
K781433 AKRON MALE EXTERNAL CATHETER
K772277 BLADDER RETENTION-CATHETHERIZATIONTRAY
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. →