SUTURE REMOVAL KIT— 510(k) K890729

Substantially Equivalent

Cypress Medical Products, Ltd.

FDA 510(k) clearance K890729 for SUTURE REMOVAL KIT, Substantially Equivalent on 1989-04-17. Applicant: Cypress Medical Products, Ltd..

Clearance details

Applicant: Cypress Medical Products, Ltd.
Product code: Code LRO
Advisory panel: General, Plastic Surgery
Date received: 1989-02-13
Decision date: 1989-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mc Henry, IL, US

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Adverse events under product code LRO

product code LRO

Injury: 975
Malfunction: 14,038
Other: 2
Total: 15,015

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.