Vlv Associates, Inc.
Vlv Associates, Inc. appears in FDA public data with 0 recalls, 12 510(k) clearances, 6 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 29, 1997.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 6
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K972957 | SA-EF MULTI-LUMEN EXTENSION SET | September 29, 1997 |
| K964876 | SA.EF(TM) INFUSION PORT II - CONNECTOR AND EXTENSION SET | February 28, 1997 |
| K955783 | VLV SA.EF INFUSION PORT EXTENSION SETS | February 7, 1996 |
| K953791 | VLV SA EF INFUSION PORT | October 30, 1995 |
| K945592 | VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGE | July 14, 1995 |
| K940406 | DISPOSABLE, AMBULATORY, INFUSION PUMPS | September 2, 1994 |
| K933364 | PROMED BIOPSY NEEDLE | February 15, 1994 |
| K922469 | PRO-LOK EXTENSION SET(S) | March 15, 1993 |
| K904217 | PRO-LOK (TM) EXTENSION SETS | October 3, 1990 |
| K901046 | VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR | June 8, 1990 |
| K901081 | PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY | June 8, 1990 |
| K860071 | HOLD-IT FRAMED ADHESIVE FILM | January 27, 1986 |