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FDA 510(k)

A O MICROSCOPE VIDEO SYSTEM

K-Number: K821865 · 1982-07-14

Decision Date1982-07-14
Product CodeIBJ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

A O MICROSCOPE VIDEO SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1982-07-14 under 510(k) number K821865. The device is classified under product code IBJ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A O MICROSCOPE VIDEO SYSTEM?

A O MICROSCOPE VIDEO SYSTEM is a medical device that received FDA 510(k) clearance on 1982-07-14. The listed applicant is Warner-Lambert Co.. The 510(k) number is K821865.

When did A O MICROSCOPE VIDEO SYSTEM receive FDA 510(k) clearance?

A O MICROSCOPE VIDEO SYSTEM received FDA 510(k) clearance on 1982-07-14, under 510(k) number K821865.

Who is the listed applicant for A O MICROSCOPE VIDEO SYSTEM?

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

What is the FDA product code for A O MICROSCOPE VIDEO SYSTEM?

The FDA product code for A O MICROSCOPE VIDEO SYSTEM is IBJ.

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 Warner-Lambert Co. 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.

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Related Devices (Code: IBJ)

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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