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FDA 510(k)

IMAGE INTENSIFIER TUBE W/HOUSING &

K-Number: K833641 · 1983-12-30

ApplicantVarian Assoc., Inc.
Decision Date1983-12-30
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGE INTENSIFIER TUBE W/HOUSING & 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 1983-12-30 under 510(k) number K833641. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAGE INTENSIFIER TUBE W/HOUSING &?

IMAGE INTENSIFIER TUBE W/HOUSING & is a medical device that received FDA 510(k) clearance on 1983-12-30. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K833641.

When did IMAGE INTENSIFIER TUBE W/HOUSING & receive FDA 510(k) clearance?

IMAGE INTENSIFIER TUBE W/HOUSING & received FDA 510(k) clearance on 1983-12-30, under 510(k) number K833641.

Who is the listed applicant for IMAGE INTENSIFIER TUBE W/HOUSING &?

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 IMAGE INTENSIFIER TUBE W/HOUSING &?

The FDA product code for IMAGE INTENSIFIER TUBE W/HOUSING & is JAA.

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Other records listing Varian Assoc., Inc. as applicant

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Related Devices (Code: JAA)

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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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