PATHFINDER MOBILE C ARM
K-Number: K981131 · 1998-06-26
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Device Summary
Frequently Asked Questions
What is the PATHFINDER MOBILE C ARM?
PATHFINDER MOBILE C ARM is a medical device that received FDA 510(k) clearance on 1998-06-26. The listed applicant is Acoma Medical Imaging, Inc.. The 510(k) number is K981131.
When did PATHFINDER MOBILE C ARM receive FDA 510(k) clearance?
PATHFINDER MOBILE C ARM received FDA 510(k) clearance on 1998-06-26, under 510(k) number K981131.
Who is the listed applicant for PATHFINDER MOBILE C ARM?
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 PATHFINDER MOBILE C ARM?
The FDA product code for PATHFINDER MOBILE C ARM is OXO.
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: OXO)
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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