DEKA JR.— 510(k) K863204

Substantially Equivalent

Deka Research & Development Corp.

FDA 510(k) clearance K863204 for DEKA JR., Substantially Equivalent on 1986-09-03. Applicant: Deka Research & Development Corp.. Device class: 2.

Clearance details

Applicant: Deka Research & Development Corp.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1986-08-19
Decision date: 1986-09-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Manchester, NH, US

Download summary PDF View on FDA.gov ↗

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