DISPOSABLE AEROSOL T
K-Number: K791538 · 1979-09-07
Advertisement
Device Summary
Frequently Asked Questions
What is the DISPOSABLE AEROSOL T?
DISPOSABLE AEROSOL T is a medical device that received FDA 510(k) clearance on 1979-09-07. The listed applicant is Hospitak, Inc.. The 510(k) number is K791538.
When did DISPOSABLE AEROSOL T receive FDA 510(k) clearance?
DISPOSABLE AEROSOL T received FDA 510(k) clearance on 1979-09-07, under 510(k) number K791538.
Who is the listed applicant for DISPOSABLE AEROSOL T?
The FDA 510(k) record lists Hospitak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE AEROSOL T?
The FDA product code for DISPOSABLE AEROSOL T is BZA.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Hospitak, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BZA)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement