THE BOOSTER— 510(k) K860698

Substantially Equivalent

Knapps Corp.

FDA 510(k) clearance K860698 for THE BOOSTER, Substantially Equivalent on 1989-02-03. Applicant: Knapps Corp.. Device class: 2.

Clearance details

Applicant: Knapps Corp.
Product code: Code LKY
Device class: Class 2
Regulation: 21 CFR 876.5020
Advisory panel: Gastroenterology, Urology
Date received: 1986-02-25
Decision date: 1989-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newark, CA, 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.