CUP OUT— 510(k) K905027

Substantially Equivalent

Anspach Mfg., Inc.

FDA 510(k) clearance K905027 for CUP OUT, Substantially Equivalent on 1991-02-05. Applicant: Anspach Mfg., Inc.. Device class: 1.

Clearance details

Applicant: Anspach Mfg., Inc.
Product code: Code HSZ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1990-11-07
Decision date: 1991-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Park, FL, US

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