FIRST AID KIT(S)— 510(k) K963298

Substantially Equivalent

Vector, Inc.

FDA 510(k) clearance K963298 for FIRST AID KIT(S), Substantially Equivalent on 1996-11-06. Applicant: Vector, Inc.. Device class: 1.

Clearance details

Applicant: Vector, Inc.
Product code: Code BYG
Device class: Class 1
Regulation: 21 CFR 868.5580
Advisory panel: Anesthesiology
Date received: 1996-08-21
Decision date: 1996-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orchard Park, NY, US

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K945472 — WESTMED PEDIATRIC AND ADULT AEROSOL MASK1995-02-07

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