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FDA 510(k)

ONE STICK Y EXTENSION SET AND VOLUMETER

K-Number: K060672 · 2006-03-31

Decision Date2006-03-31
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ONE STICK Y EXTENSION SET AND VOLUMETER is the device name listed in this FDA 510(k) record. The listed applicant is One Stick, LLC. It received FDA 510(k) clearance on 2006-03-31 under 510(k) number K060672. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONE STICK Y EXTENSION SET AND VOLUMETER?

ONE STICK Y EXTENSION SET AND VOLUMETER is a medical device that received FDA 510(k) clearance on 2006-03-31. The listed applicant is One Stick, LLC. The 510(k) number is K060672.

When did ONE STICK Y EXTENSION SET AND VOLUMETER receive FDA 510(k) clearance?

ONE STICK Y EXTENSION SET AND VOLUMETER received FDA 510(k) clearance on 2006-03-31, under 510(k) number K060672.

Who is the listed applicant for ONE STICK Y EXTENSION SET AND VOLUMETER?

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

What is the FDA product code for ONE STICK Y EXTENSION SET AND VOLUMETER?

The FDA product code for ONE STICK Y EXTENSION SET AND VOLUMETER is FPA.

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.

Related Devices (Code: FPA)

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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