Neotech Products, Inc.
Neotech Products, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 3, 2002.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K011564 | NEOLEAD | January 3, 2002 |
| K931727 | URINARY DRAINAGE BAG CADDY | July 23, 1993 |
| K921024 | URO-TOTE LEG BAG | September 2, 1992 |
| K890425 | NEOTECH MUCUS TRAP W/CATHETER | April 19, 1989 |
| K882203 | NEOTECH UNIVERSAL ADAPTER | June 17, 1988 |
| K880487 | NEOTECH MECONIUM ASPIRATOR (STERILE) | May 6, 1988 |