NEEDLE GUIDE ATTACHMENT— 510(k) K811931

Substantially Equivalent

Technicare Corp.

FDA 510(k) clearance K811931 for NEEDLE GUIDE ATTACHMENT, Substantially Equivalent on 1981-08-18. Applicant: Technicare Corp..

Clearance details

Applicant: Technicare Corp.
Product code: Code IYO
Advisory panel: Radiology
Date received: 1981-07-06
Decision date: 1981-08-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

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.