AEROS ASPIRATOR
K-Number: K952103 · 1995-07-31
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Device Summary
Frequently Asked Questions
What is the AEROS ASPIRATOR?
AEROS ASPIRATOR is a medical device that received FDA 510(k) clearance on 1995-07-31. The listed applicant is Aeros Instruments, Inc.. The 510(k) number is K952103.
When did AEROS ASPIRATOR receive FDA 510(k) clearance?
AEROS ASPIRATOR received FDA 510(k) clearance on 1995-07-31, under 510(k) number K952103.
Who is the listed applicant for AEROS ASPIRATOR?
The FDA 510(k) record lists Aeros Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AEROS ASPIRATOR?
The FDA product code for AEROS ASPIRATOR is BTA.
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 Aeros Instruments, 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: BTA)
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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