VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGE— 510(k) K945592

Substantially Equivalent

Vlv Associates, Inc.

FDA 510(k) clearance K945592 for VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGE, Substantially Equivalent on 1995-07-14. Applicant: Vlv Associates, Inc..

Clearance details

Applicant: Vlv Associates, Inc.
Product code: Code FMF
Advisory panel: General Hospital
Date received: 1994-11-14
Decision date: 1995-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: East Hanover, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.