UNIQUE NEEDLE— 510(k) K950245

Substantially Equivalent

Unique Management Ent., Inc.

FDA 510(k) clearance K950245 for UNIQUE NEEDLE, Substantially Equivalent on 1995-12-06. Applicant: Unique Management Ent., Inc..

Clearance details

Applicant: Unique Management Ent., Inc.
Product code: Code FMF
Advisory panel: General Hospital
Date received: 1995-01-20
Decision date: 1995-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Albany, NY, 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.