FLO CONTROL— 510(k) K822891

Substantially Equivalent

Dna Medical, Inc.

FDA 510(k) clearance K822891 for FLO CONTROL, Substantially Equivalent on 1982-11-24. Applicant: Dna Medical, Inc.. Device class: 2.

Clearance details

Applicant: Dna Medical, Inc.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1982-09-28
Decision date: 1982-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: UT, US

Download summary PDF View on FDA.gov ↗

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