F/C/W TUBESTAND
K-Number: K941017 · 1994-07-29
Advertisement
Device Summary
Frequently Asked Questions
What is the F/C/W TUBESTAND?
F/C/W TUBESTAND is a medical device that received FDA 510(k) clearance on 1994-07-29. The listed applicant is Acoma Medical Imaging, Inc.. The 510(k) number is K941017.
When did F/C/W TUBESTAND receive FDA 510(k) clearance?
F/C/W TUBESTAND received FDA 510(k) clearance on 1994-07-29, under 510(k) number K941017.
Who is the listed applicant for F/C/W TUBESTAND?
The FDA 510(k) record lists Acoma Medical Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for F/C/W TUBESTAND?
The FDA product code for F/C/W TUBESTAND is IYB.
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 Acoma Medical Imaging, 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: IYB)
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.
Advertisement