VIDICAM 200
K-Number: K812613 · 1981-12-08
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement