GUIDEWIRES, VARIOUS TYPES— 510(k) K920884

Substantially Equivalent

Acme-Monaco Corp.

FDA 510(k) clearance K920884 for GUIDEWIRES, VARIOUS TYPES, Substantially Equivalent on 1992-08-19. Applicant: Acme-Monaco Corp..

Clearance details

Applicant: Acme-Monaco Corp.
Product code: Code DQX
Advisory panel: Cardiovascular
Date received: 1992-01-02
Decision date: 1992-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crisfield, MD, US

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Adverse events under product code DQX

product code DQX

Death: 298
Injury: 4,385
Malfunction: 7,203
Other: 5
Total: 11,891

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.