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FDA 510(k)

VIDEO PLUS SYSTEM, SERIES 95000

K-Number: K992666 · 1999-10-13

ApplicantCamtronics, Ltd.
Decision Date1999-10-13
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDEO PLUS SYSTEM, SERIES 95000 is the device name listed in this FDA 510(k) record. The listed applicant is Camtronics, Ltd.. It received FDA 510(k) clearance on 1999-10-13 under 510(k) number K992666. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDEO PLUS SYSTEM, SERIES 95000?

VIDEO PLUS SYSTEM, SERIES 95000 is a medical device that received FDA 510(k) clearance on 1999-10-13. The listed applicant is Camtronics, Ltd.. The 510(k) number is K992666.

When did VIDEO PLUS SYSTEM, SERIES 95000 receive FDA 510(k) clearance?

VIDEO PLUS SYSTEM, SERIES 95000 received FDA 510(k) clearance on 1999-10-13, under 510(k) number K992666.

Who is the listed applicant for VIDEO PLUS SYSTEM, SERIES 95000?

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 SYSTEM, SERIES 95000?

The FDA product code for VIDEO PLUS SYSTEM, SERIES 95000 is LLZ.

Related Clinical Trials

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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 95000K992259ECHOCARDIOGRAPHY SYSTEM SERIES 95000K990066CCD CAMERA, MODEL 9000K955519ANALYTICAL REVIEW STATIONK954159DIGITAL IMAGING SYSTEM

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Related Devices (Code: LLZ)

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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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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