Latex Ind., Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
FDA 510(k) Regulatory Record - Latex Ind., Inc. Gastroenterology & Urology ✕
14 devices
Cleared
Jul 31, 1981
AKRON URINARY DRAINAGE BAT
Gastroenterology & Urology
10d
Cleared
Feb 25, 1981
UROLOGICAL CATHETERS
Gastroenterology & Urology
23d
Cleared
Nov 05, 1979
BLADDER RETENTION CATHETERIZATION TRAY
Gastroenterology & Urology
70d
Cleared
Jan 22, 1979
CATHETER, AKRON FOLEY TEFLON
Gastroenterology & Urology
98d
Cleared
Nov 03, 1978
AKRON MALE EXTERNAL CATHETER
Gastroenterology & Urology
74d
Cleared
Mar 02, 1978
BLADDER RETENTION-CATHETHERIZATIONTRAY
Gastroenterology & Urology
83d
Cleared
Feb 24, 1978
CATHETERIZATION KIT 732016-732018
Gastroenterology & Urology
64d
Cleared
Feb 24, 1978
BLADDER KIT - 734000
Gastroenterology & Urology
64d
Cleared
Feb 24, 1978
ROBINSON KIT - 750014 & 750016
Gastroenterology & Urology
64d
Cleared
Feb 24, 1978
CATH TRAY W/OUT CATHETER
Gastroenterology & Urology
7d
Cleared
Feb 24, 1978
BLADDER CATH KIT W/OUT CATHETER
Gastroenterology & Urology
7d
Cleared
Sep 20, 1977
AKRO-SIL FOLEY KIT 30CC
Gastroenterology & Urology
22d
Cleared
Sep 20, 1977
AKRO-SIL FOLEY KIT 5CC
Gastroenterology & Urology
22d
Cleared
Sep 20, 1977
CATH-CARE TRAY
Gastroenterology & Urology
22d