PDB II— 510(k) K830289

Substantially Equivalent

J.A. Gerber Therapeutical, Ltd.

FDA 510(k) clearance K830289 for PDB II, Substantially Equivalent on 1983-03-25. Applicant: J.A. Gerber Therapeutical, Ltd.. Device class: 1.

Clearance details

Applicant: J.A. Gerber Therapeutical, Ltd.
Product code: Code INQ
Device class: Class 1
Regulation: 21 CFR 890.3760
Advisory panel: Physical Medicine
Date received: 1983-01-27
Decision date: 1983-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.