FDA 510(k)

FLUOROSCOPE, C-ARM

K-Number: K770333 · 1977-03-01

Decision Date1977-03-01

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

FLUOROSCOPE, C-ARM is the device name listed in this FDA 510(k) record. The listed applicant is Litton Medical Systems. It received FDA 510(k) clearance on 1977-03-01 under 510(k) number K770333. 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 FLUOROSCOPE, C-ARM?

FLUOROSCOPE, C-ARM is a medical device that received FDA 510(k) clearance on 1977-03-01. The listed applicant is Litton Medical Systems. The 510(k) number is K770333.

When did FLUOROSCOPE, C-ARM receive FDA 510(k) clearance?

FLUOROSCOPE, C-ARM received FDA 510(k) clearance on 1977-03-01, under 510(k) number K770333.

Who is the listed applicant for FLUOROSCOPE, C-ARM?

The FDA 510(k) record lists Litton Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUOROSCOPE, C-ARM?

The FDA product code for FLUOROSCOPE, C-ARM is JAA.

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Other records listing Litton Medical Systems as applicant

K770334TILTING X-RAY TABLE K770336X-RAY TUBE, ROTATING ANODE K770338X-RAY CONTROL & X-RAY HV GENERATOR K770337FLUOROSCOPIC ASSEMBLY, IMAGE INTENS.K770335COLLIMATOR, AUTOMATIC K760569THREE PHASE X-RAY CONTROLS & HV GENERATORS

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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.