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FDA 510(k)

Alamo® C

K-Number: K173128 · 2018-03-22

Decision Date2018-03-22
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Alamo® C is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Partners, LLC. It received FDA 510(k) clearance on 2018-03-22 under 510(k) number K173128. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Alamo® C?

Alamo® C is a medical device that received FDA 510(k) clearance on 2018-03-22. The listed applicant is Alliance Partners, LLC. The 510(k) number is K173128.

When did Alamo® C receive FDA 510(k) clearance?

Alamo® C received FDA 510(k) clearance on 2018-03-22, under 510(k) number K173128.

Who is the listed applicant for Alamo® C?

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

What is the FDA product code for Alamo® C?

The FDA product code for Alamo® C is ODP.

Other records listing Alliance Partners, LLC 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: ODP)

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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