ALTRACLUDE— 510(k) K811303

Substantially Equivalent

R&H Medical, Inc.

FDA 510(k) clearance K811303 for ALTRACLUDE, Substantially Equivalent on 1981-06-16. Applicant: R&H Medical, Inc.. Device class: 1.

Clearance details

Applicant: R&H Medical, Inc.
Product code: Code KDC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1981-05-11
Decision date: 1981-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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