KLEENSPEC— 510(k) K941272

Substantially Equivalent

Welch Allyn, Inc.

FDA 510(k) clearance K941272 for KLEENSPEC, Substantially Equivalent on 1994-08-02. Applicant: Welch Allyn, Inc.. Device class: 2.

Clearance details

Applicant: Welch Allyn, Inc.
Product code: Code HIB
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1994-03-16
Decision date: 1994-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skaneateles Falls, NY, 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.