AUKUSLEEVE— 510(k) K930094

Substantially Equivalent

Aukland Medical Plastics, Inc.

FDA 510(k) clearance K930094 for AUKUSLEEVE, Substantially Equivalent on 1993-10-20. Applicant: Aukland Medical Plastics, Inc.. Device class: 1.

Clearance details

Applicant: Aukland Medical Plastics, Inc.
Product code: Code EJB
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1993-01-08
Decision date: 1993-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cary, NC, US

Download summary PDF View on FDA.gov ↗

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More clearances from Aukland Medical Plastics, Inc.

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Data sourced from openFDA. This site is unofficial and independent of the FDA.