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FDA 510(k)

VIDICAM 200

K-Number: K812613 · 1981-12-08

Decision Date1981-12-08
Product CodeIZJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDICAM 200 is the device name listed in this FDA 510(k) record. The listed applicant is Diversified P.A.. It received FDA 510(k) clearance on 1981-12-08 under 510(k) number K812613. The device is classified under product code IZJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDICAM 200?

VIDICAM 200 is a medical device that received FDA 510(k) clearance on 1981-12-08. The listed applicant is Diversified P.A.. The 510(k) number is K812613.

When did VIDICAM 200 receive FDA 510(k) clearance?

VIDICAM 200 received FDA 510(k) clearance on 1981-12-08, under 510(k) number K812613.

Who is the listed applicant for VIDICAM 200?

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

What is the FDA product code for VIDICAM 200?

The FDA product code for VIDICAM 200 is IZJ.

Related Clinical Trials

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.

Other records listing Diversified P.A. 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.

Related Devices (Code: IZJ)

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.

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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