HARE FOLDING BACK EMERGENCY STRETCHER— 510(k) K902503

Substantially Equivalent

Dyna Corp.

FDA 510(k) clearance K902503 for HARE FOLDING BACK EMERGENCY STRETCHER, Substantially Equivalent on 1990-06-26. Applicant: Dyna Corp..

Clearance details

Applicant: Dyna Corp.
Product code: Code FPO
Advisory panel: General Hospital
Date received: 1990-06-05
Decision date: 1990-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carlsbad, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FPO

product code FPO

Death: 29
Injury: 254
Malfunction: 5,054
Other: 10
Total: 5,347

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.