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FDA 510(k)

FLOUROSCOPE, MOBILE C-ARM IMAGE INTENS.

K-Number: K760429 · 1976-08-23

ApplicantVarian Assoc., Inc.
Decision Date1976-08-23
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLOUROSCOPE, MOBILE C-ARM IMAGE INTENS. 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 1976-08-23 under 510(k) number K760429. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOUROSCOPE, MOBILE C-ARM IMAGE INTENS.?

FLOUROSCOPE, MOBILE C-ARM IMAGE INTENS. is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K760429.

When did FLOUROSCOPE, MOBILE C-ARM IMAGE INTENS. receive FDA 510(k) clearance?

FLOUROSCOPE, MOBILE C-ARM IMAGE INTENS. received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760429.

Who is the listed applicant for FLOUROSCOPE, MOBILE C-ARM IMAGE INTENS.?

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 FLOUROSCOPE, MOBILE C-ARM IMAGE INTENS.?

The FDA product code for FLOUROSCOPE, MOBILE C-ARM IMAGE INTENS. is OXO.

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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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