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FDA 510(k)

VIDICAM VIDEO REPROGRAPH

K-Number: K790395 · 1979-03-28

ApplicantVidicam
Decision Date1979-03-28
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDICAM VIDEO REPROGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Vidicam. It received FDA 510(k) clearance on 1979-03-28 under 510(k) number K790395. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDICAM VIDEO REPROGRAPH?

VIDICAM VIDEO REPROGRAPH is a medical device that received FDA 510(k) clearance on 1979-03-28. The listed applicant is Vidicam. The 510(k) number is K790395.

When did VIDICAM VIDEO REPROGRAPH receive FDA 510(k) clearance?

VIDICAM VIDEO REPROGRAPH received FDA 510(k) clearance on 1979-03-28, under 510(k) number K790395.

Who is the listed applicant for VIDICAM VIDEO REPROGRAPH?

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

What is the FDA product code for VIDICAM VIDEO REPROGRAPH?

The FDA product code for VIDICAM VIDEO REPROGRAPH is JAK.

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Related Devices (Code: JAK)

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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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