AEROSOL DELIVERY SYSTEMS— 510(k) K920842

Substantially Equivalent

Hospitak, Inc.

FDA 510(k) clearance K920842 for AEROSOL DELIVERY SYSTEMS, Substantially Equivalent on 1992-05-15. Applicant: Hospitak, Inc.. Device class: 1.

Clearance details

Applicant: Hospitak, Inc.
Product code: Code LRD
Device class: Class 1
Regulation: 21 CFR 874.5220
Advisory panel: Ear, Nose, Throat
Date received: 1992-02-24
Decision date: 1992-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lindenhurst, NY, US

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