A O MICROSCOPE VIDEO SYSTEM
K-Number: K821865 · 1982-07-14
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Device Summary
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.
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
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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