Latex Ind., Inc.
Latex Ind., Inc. appears in FDA public data with 0 recalls, 14 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jul 31, 1981.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K812058 | AKRON URINARY DRAINAGE BAT | Jul 31, 1981 |
| K810281 | UROLOGICAL CATHETERS | Feb 25, 1981 |
| K791674 | BLADDER RETENTION CATHETERIZATION TRAY | Nov 5, 1979 |
| K781751 | CATHETER, AKRON FOLEY TEFLON | Jan 22, 1979 |
| K781433 | AKRON MALE EXTERNAL CATHETER | Nov 3, 1978 |
| K772277 | BLADDER RETENTION-CATHETHERIZATIONTRAY | Mar 2, 1978 |
| K772341 | BLADDER KIT - 734000 | Feb 24, 1978 |
| K772340 | CATHETERIZATION KIT 732016-732018 | Feb 24, 1978 |
| K780268 | BLADDER CATH KIT W/OUT CATHETER | Feb 24, 1978 |
| K780267 | CATH TRAY W/OUT CATHETER | Feb 24, 1978 |
| K772342 | ROBINSON KIT - 750014 & 750016 | Feb 24, 1978 |
| K771652 | CATH-CARE TRAY | Sep 20, 1977 |
| K771650 | AKRO-SIL FOLEY KIT 30CC | Sep 20, 1977 |
| K771651 | AKRO-SIL FOLEY KIT 5CC | Sep 20, 1977 |