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FDA 510(k)

COORDINATUS, HORIZONTAL RADIOGRAPHOC

K-Number: K790743 · 1979-04-23

ApplicantPausch Corp.
Decision Date1979-04-23
Product CodeKXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COORDINATUS, HORIZONTAL RADIOGRAPHOC is the device name listed in this FDA 510(k) record. The listed applicant is Pausch Corp.. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790743. The device is classified under product code KXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COORDINATUS, HORIZONTAL RADIOGRAPHOC?

COORDINATUS, HORIZONTAL RADIOGRAPHOC is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Pausch Corp.. The 510(k) number is K790743.

When did COORDINATUS, HORIZONTAL RADIOGRAPHOC receive FDA 510(k) clearance?

COORDINATUS, HORIZONTAL RADIOGRAPHOC received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790743.

Who is the listed applicant for COORDINATUS, HORIZONTAL RADIOGRAPHOC?

The FDA 510(k) record lists Pausch Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COORDINATUS, HORIZONTAL RADIOGRAPHOC?

The FDA product code for COORDINATUS, HORIZONTAL RADIOGRAPHOC is KXJ.

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 Pausch Corp. 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.

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Related Devices (Code: KXJ)

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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