EPISCOPE, MODEL 47300— 510(k) K920103

Substantially Equivalent

Welch Allyn, Inc.

FDA 510(k) clearance K920103 for EPISCOPE, MODEL 47300, Substantially Equivalent on 1992-04-28. Applicant: Welch Allyn, Inc.. Device class: 1.

Clearance details

Applicant: Welch Allyn, Inc.
Product code: Code KZF
Device class: Class 1
Regulation: 21 CFR 880.6320
Advisory panel: General Hospital
Date received: 1992-01-09
Decision date: 1992-04-28
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.