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FDA 510(k)

FREEDOM ASPIRATOR, MODEL 6000

K-Number: K944116 · 1994-09-07

Decision Date1994-09-07
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FREEDOM ASPIRATOR, MODEL 6000 is the device name listed in this FDA 510(k) record. The listed applicant is Stackhouse, Inc.. It received FDA 510(k) clearance on 1994-09-07 under 510(k) number K944116. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREEDOM ASPIRATOR, MODEL 6000?

FREEDOM ASPIRATOR, MODEL 6000 is a medical device that received FDA 510(k) clearance on 1994-09-07. The listed applicant is Stackhouse, Inc.. The 510(k) number is K944116.

When did FREEDOM ASPIRATOR, MODEL 6000 receive FDA 510(k) clearance?

FREEDOM ASPIRATOR, MODEL 6000 received FDA 510(k) clearance on 1994-09-07, under 510(k) number K944116.

Who is the listed applicant for FREEDOM ASPIRATOR, MODEL 6000?

The FDA 510(k) record lists Stackhouse, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FREEDOM ASPIRATOR, MODEL 6000?

The FDA product code for FREEDOM ASPIRATOR, MODEL 6000 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 Stackhouse, 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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