STRETCHER, WHEELED, MECHANICAL— 510(k) K873181

Substantially Equivalent

Cambridge Technologies, Inc.

FDA 510(k) clearance K873181 for STRETCHER, WHEELED, MECHANICAL, Substantially Equivalent on 1987-10-09. Applicant: Cambridge Technologies, Inc..

Clearance details

Applicant: Cambridge Technologies, Inc.
Product code: Code FPO
Advisory panel: General Hospital
Date received: 1987-08-12
Decision date: 1987-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cambridge, MD, US

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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.