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FDA 510(k)

JOINT MOTON IMAGER(TM)

K-Number: K902583 · 1990-09-27

ApplicantConcord Imaging, Ltd.
Decision Date1990-09-27
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

JOINT MOTON IMAGER(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Concord Imaging, Ltd.. It received FDA 510(k) clearance on 1990-09-27 under 510(k) number K902583. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOINT MOTON IMAGER(TM)?

JOINT MOTON IMAGER(TM) is a medical device that received FDA 510(k) clearance on 1990-09-27. The listed applicant is Concord Imaging, Ltd.. The 510(k) number is K902583.

When did JOINT MOTON IMAGER(TM) receive FDA 510(k) clearance?

JOINT MOTON IMAGER(TM) received FDA 510(k) clearance on 1990-09-27, under 510(k) number K902583.

Who is the listed applicant for JOINT MOTON IMAGER(TM)?

The FDA 510(k) record lists Concord Imaging, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JOINT MOTON IMAGER(TM)?

The FDA product code for JOINT MOTON IMAGER(TM) is JAA.

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Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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