PMD SYSTEM-20— 510(k) K883390

Substantially Equivalent

Datatek, Inc.

FDA 510(k) clearance K883390 for PMD SYSTEM-20, Substantially Equivalent on 1988-10-25. Applicant: Datatek, Inc.. Device class: 1.

Clearance details

Applicant: Datatek, Inc.
Product code: Code KMI
Device class: Class 1
Regulation: 21 CFR 880.2400
Advisory panel: General Hospital
Date received: 1988-08-09
Decision date: 1988-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shreveport, LA, 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.