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FDA 510(k)

FLUOROSCOPIC IMAGE INTENSIFIER

K-Number: K840621 · 1984-06-05

ApplicantPhoenix Radiology, Ltd.
Decision Date1984-06-05
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLUOROSCOPIC IMAGE INTENSIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Radiology, Ltd.. It received FDA 510(k) clearance on 1984-06-05 under 510(k) number K840621. 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 FLUOROSCOPIC IMAGE INTENSIFIER?

FLUOROSCOPIC IMAGE INTENSIFIER is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is Phoenix Radiology, Ltd.. The 510(k) number is K840621.

When did FLUOROSCOPIC IMAGE INTENSIFIER receive FDA 510(k) clearance?

FLUOROSCOPIC IMAGE INTENSIFIER received FDA 510(k) clearance on 1984-06-05, under 510(k) number K840621.

Who is the listed applicant for FLUOROSCOPIC IMAGE INTENSIFIER?

The FDA 510(k) record lists Phoenix Radiology, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUOROSCOPIC IMAGE INTENSIFIER?

The FDA product code for FLUOROSCOPIC IMAGE INTENSIFIER is JAA.

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Related Devices (Code: JAA)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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