Latex Ind., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Latex Ind., Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Latex Ind., Inc. has 14 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1977 to 1981.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Latex Ind., Inc.
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