MASTER SCREEN PNUEMO— 510(k) K933839

Substantially Equivalent

Erich Jaeger, Inc.

FDA 510(k) clearance K933839 for MASTER SCREEN PNUEMO, Substantially Equivalent on 1994-03-07. Applicant: Erich Jaeger, Inc.. Device class: 2.

Clearance details

Applicant: Erich Jaeger, Inc.
Product code: Code BTY
Device class: Class 2
Regulation: 21 CFR 868.1890
Advisory panel: Anesthesiology
Date received: 1993-08-05
Decision date: 1994-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockford, IL, 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.