NEEDLE GUARD(TM)— 510(k) K890473

Substantially Equivalent

Martech Medical Products, Inc.

FDA 510(k) clearance K890473 for NEEDLE GUARD(TM), Substantially Equivalent on 1989-04-03. Applicant: Martech Medical Products, Inc..

Clearance details

Applicant: Martech Medical Products, Inc.
Product code: Code FMI
Advisory panel: General Hospital
Date received: 1989-01-31
Decision date: 1989-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Riverside, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMI

product code FMI

Death: 28
Injury: 1,517
Malfunction: 23,981
Other: 18
Total: 25,544

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.