VITAPEN— 510(k) K924447

Substantially Equivalent

Vitajet Corp.

FDA 510(k) clearance K924447 for VITAPEN, Substantially Equivalent on 1993-09-27. Applicant: Vitajet Corp.. Device class: 1.

Clearance details

Applicant: Vitajet Corp.
Product code: Code KZF
Device class: Class 1
Regulation: 21 CFR 880.6320
Advisory panel: General Hospital
Date received: 1992-09-01
Decision date: 1993-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laguna Hills, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Vitajet Corp.

K962625 — VITAJET1996-12-10
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Data sourced from openFDA. This site is unofficial and independent of the FDA.