ASPIRE— 510(k) K936110

Substantially Equivalent

Dura Pharmaceuticals, Inc.

FDA 510(k) clearance K936110 for ASPIRE, Substantially Equivalent on 1995-03-23. Applicant: Dura Pharmaceuticals, Inc.. Device class: 2.

Clearance details

Applicant: Dura Pharmaceuticals, Inc.
Product code: Code BZH
Device class: Class 2
Regulation: 21 CFR 868.1860
Advisory panel: Anesthesiology
Date received: 1993-12-23
Decision date: 1995-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, 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.