AEROSOL T ADAPTER, #752
K-Number: K770585 · 1977-04-05
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Device Summary
Frequently Asked Questions
What is the AEROSOL T ADAPTER, #752?
AEROSOL T ADAPTER, #752 is a medical device that received FDA 510(k) clearance on 1977-04-05. The listed applicant is Surgicot, Inc.. The 510(k) number is K770585.
When did AEROSOL T ADAPTER, #752 receive FDA 510(k) clearance?
AEROSOL T ADAPTER, #752 received FDA 510(k) clearance on 1977-04-05, under 510(k) number K770585.
Who is the listed applicant for AEROSOL T ADAPTER, #752?
The FDA 510(k) record lists Surgicot, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AEROSOL T ADAPTER, #752?
The FDA product code for AEROSOL T ADAPTER, #752 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 Surgicot, 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.
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