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FDA 510(k)

PATHFINDER MOBILE C ARM

K-Number: K981131 · 1998-06-26

Decision Date1998-06-26
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PATHFINDER MOBILE C ARM is the device name listed in this FDA 510(k) record. The listed applicant is Acoma Medical Imaging, Inc.. It received FDA 510(k) clearance on 1998-06-26 under 510(k) number K981131. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 13 devices →

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

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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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