SURGITEK FLAT T-SPAN— 510(k) K884746

Name: FDA 510(k) clearance K884746
Creator: U.S. Food and Drug Administration
Published: 1989-08-10

Substantially Equivalent

Medical Engineering Corp.

FDA 510(k) clearance K884746 for SURGITEK FLAT T-SPAN, Substantially Equivalent on 1989-08-10. Applicant: Medical Engineering Corp.. Device class: Unclassified.

Clearance details

Applicant: Medical Engineering Corp.
Product code: Code LCJ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1988-11-14
Decision date: 1989-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Racine, WI, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LCJ

product code LCJ

Injury: 2,704
Other: 2
Total: 2,706

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.