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FDA 510(k)

6MV PORT FILM CAPABILITY OPTION

K-Number: K802808 · 1981-01-07

ApplicantVarian Assoc., Inc.
Decision Date1981-01-07
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

6MV PORT FILM CAPABILITY OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1981-01-07 under 510(k) number K802808. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 6MV PORT FILM CAPABILITY OPTION?

6MV PORT FILM CAPABILITY OPTION is a medical device that received FDA 510(k) clearance on 1981-01-07. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K802808.

When did 6MV PORT FILM CAPABILITY OPTION receive FDA 510(k) clearance?

6MV PORT FILM CAPABILITY OPTION received FDA 510(k) clearance on 1981-01-07, under 510(k) number K802808.

Who is the listed applicant for 6MV PORT FILM CAPABILITY OPTION?

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

What is the FDA product code for 6MV PORT FILM CAPABILITY OPTION?

The FDA product code for 6MV PORT FILM CAPABILITY OPTION is IYE.

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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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