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FDA 510(k)

VIDEO PLUS MODELS VP500, VP500A AND VP1000

K-Number: K871743 · 1987-06-22

ApplicantCamtronics, Ltd.
Decision Date1987-06-22
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDEO PLUS MODELS VP500, VP500A AND VP1000 is the device name listed in this FDA 510(k) record. The listed applicant is Camtronics, Ltd.. It received FDA 510(k) clearance on 1987-06-22 under 510(k) number K871743. 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 VIDEO PLUS MODELS VP500, VP500A AND VP1000?

VIDEO PLUS MODELS VP500, VP500A AND VP1000 is a medical device that received FDA 510(k) clearance on 1987-06-22. The listed applicant is Camtronics, Ltd.. The 510(k) number is K871743.

When did VIDEO PLUS MODELS VP500, VP500A AND VP1000 receive FDA 510(k) clearance?

VIDEO PLUS MODELS VP500, VP500A AND VP1000 received FDA 510(k) clearance on 1987-06-22, under 510(k) number K871743.

Who is the listed applicant for VIDEO PLUS MODELS VP500, VP500A AND VP1000?

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

What is the FDA product code for VIDEO PLUS MODELS VP500, VP500A AND VP1000?

The FDA product code for VIDEO PLUS MODELS VP500, VP500A AND VP1000 is JAA.

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Other records listing Camtronics, Ltd. 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.

K021236SURGERY AND ACCESSORIESK013032PHYSIOLOG, SERIES 95000K992666VIDEO PLUS SYSTEM, SERIES 95000K992259ECHOCARDIOGRAPHY SYSTEM SERIES 95000K990066CCD CAMERA, MODEL 9000K955519ANALYTICAL REVIEW STATION

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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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