ANALGRAPH— 510(k) K941801

Substantially Equivalent

Sandhill Scientific, Inc.

FDA 510(k) clearance K941801 for ANALGRAPH, Substantially Equivalent on 1995-09-08. Applicant: Sandhill Scientific, Inc.. Device class: 2.

Clearance details

Applicant: Sandhill Scientific, Inc.
Product code: Code KLA
Device class: Class 2
Regulation: 21 CFR 876.1725
Advisory panel: Gastroenterology, Urology
Date received: 1994-04-12
Decision date: 1995-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Littleton, CO, 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.