ONE STICK Y EXTENSION SET AND VOLUMETER
K-Number: K060672 · 2006-03-31
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Device Summary
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
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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