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FDA 510(k)

CAMTEX 1000

K-Number: K840134 · 1984-03-16

ApplicantDigital Imaging Co. of America
Decision Date1984-03-16
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAMTEX 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Digital Imaging Co. of America. It received FDA 510(k) clearance on 1984-03-16 under 510(k) number K840134. 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 CAMTEX 1000?

CAMTEX 1000 is a medical device that received FDA 510(k) clearance on 1984-03-16. The listed applicant is Digital Imaging Co. of America. The 510(k) number is K840134.

When did CAMTEX 1000 receive FDA 510(k) clearance?

CAMTEX 1000 received FDA 510(k) clearance on 1984-03-16, under 510(k) number K840134.

Who is the listed applicant for CAMTEX 1000?

The FDA 510(k) record lists Digital Imaging Co. of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAMTEX 1000?

The FDA product code for CAMTEX 1000 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

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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