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FDA 510(k)

PENUMBRA ASPIRATION PUMP, MODEL 115V

K-Number: K051758 · 2005-08-17

Decision Date2005-08-17
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PENUMBRA ASPIRATION PUMP, MODEL 115V is the device name listed in this FDA 510(k) record. The listed applicant is Penumbra, Inc.. It received FDA 510(k) clearance on 2005-08-17 under 510(k) number K051758. 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 PENUMBRA ASPIRATION PUMP, MODEL 115V?

PENUMBRA ASPIRATION PUMP, MODEL 115V is a medical device that received FDA 510(k) clearance on 2005-08-17. The listed applicant is Penumbra, Inc.. The 510(k) number is K051758.

When did PENUMBRA ASPIRATION PUMP, MODEL 115V receive FDA 510(k) clearance?

PENUMBRA ASPIRATION PUMP, MODEL 115V received FDA 510(k) clearance on 2005-08-17, under 510(k) number K051758.

Who is the listed applicant for PENUMBRA ASPIRATION PUMP, MODEL 115V?

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

What is the FDA product code for PENUMBRA ASPIRATION PUMP, MODEL 115V?

The FDA product code for PENUMBRA ASPIRATION PUMP, MODEL 115V 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 Penumbra, 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.

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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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