LOUISVILLE CLAMP PRODUCT #65-172— 510(k) K770503

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K770503 for LOUISVILLE CLAMP PRODUCT #65-172, Substantially Equivalent on 1977-03-30. Applicant: Edward Weck, Inc..

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code DXC
Advisory panel: Cardiovascular
Date received: 1977-03-16
Decision date: 1977-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DXC

product code DXC

Death: 14
Injury: 442
Malfunction: 2,209
Other: 1
Total: 2,666

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.