AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO— 510(k) K001502

Name: FDA 510(k) clearance K001502
Creator: U.S. Food and Drug Administration
Published: 2000-07-12

Substantially Equivalent

Erich Jaeger GmbH

FDA 510(k) clearance K001502 for AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO, Substantially Equivalent on 2000-07-12. Applicant: Erich Jaeger GmbH. Device class: 2.

Clearance details

Applicant: Erich Jaeger GmbH
Product code: Code BZC
Device class: Class 2
Regulation: 21 CFR 868.1880
Advisory panel: Anesthesiology
Date received: 2000-05-15
Decision date: 2000-07-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Yorba Linda, CA, US

Download summary PDF View on FDA.gov ↗

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