VLV Associates, Inc.
Whippany, NJ, US
VLV ASSOCIATES, INC. appears in FDA device records in Whippany, NJ. FDA records list 12 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 12 510(k) clearances for VLV Associates, Inc. between 1986 and 1997. The busiest year on record is 1990, with 3. The most recent is 1997, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1986 | 1 |
| 1990 | 3 |
| 1993 | 1 |
| 1994 | 2 |
| 1995 | 2 |
| 1996 | 1 |
| 1997 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K972957 | SA-EF MULTI-LUMEN EXTENSION SET | FPA | Substantially Equivalent | |
| K964876 | SA.EF(TM) INFUSION PORT II - CONNECTOR AND EXTENSION SET | FPA | Substantially Equivalent | |
| K955783 | VLV SA.EF INFUSION PORT EXTENSION SETS | FPA | Substantially Equivalent | |
| K953791 | VLV SA EF INFUSION PORT | FPA | Substantially Equivalent | |
| K945592 | VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGE | FMF | Substantially Equivalent | |
| K940406 | DISPOSABLE, AMBULATORY, INFUSION PUMPS | MEB | Substantially Equivalent - Subject to Tracking Reg. | |
| K933364 | PROMED BIOPSY NEEDLE | DWO | Substantially Equivalent | |
| K922469 | PRO-LOK EXTENSION SET(S) | FPA | Substantially Equivalent | |
| K904217 | PRO-LOK (TM) EXTENSION SETS | FPA | Substantially Equivalent | |
| K901081 | PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY | FPA | Substantially Equivalent | |
| K901046 | VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR | FPA | Substantially Equivalent | |
| K860071 | HOLD-IT FRAMED ADHESIVE FILM | KMK | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 2245539 | 2245539 | VLV ASSOCIATES, INC. | 34 Troy Rd, Whippany, NJ 07981 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- EYKConnector, Ureteral Catheter
- KMKDevice, Intravascular Catheter Securement
- GAANeedle, Aspiration And Injection, Disposable
- DWONeedle, Biopsy, Cardiovascular
- PTINon-Coring (Huber) Needle
- MEBPump, Infusion, Elastomeric
- KGWRing (Wound Protector), Drape Retention, Internal
- FPASet, Administration, Intravascular
- FMFSyringe, Piston
- IYOSystem, Imaging, Pulsed Echo, Ultrasonic
- KGNWound Dressing With Animal-Derived Material(S)
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain