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FDA 510(k)

C-ARM CEILING CRANE FT-2

K-Number: K840225 · 1984-03-22

ApplicantMedicor USA , Ltd.
Decision Date1984-03-22
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

C-ARM CEILING CRANE FT-2 is the device name listed in this FDA 510(k) record. The listed applicant is Medicor USA , Ltd.. It received FDA 510(k) clearance on 1984-03-22 under 510(k) number K840225. 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 C-ARM CEILING CRANE FT-2?

C-ARM CEILING CRANE FT-2 is a medical device that received FDA 510(k) clearance on 1984-03-22. The listed applicant is Medicor USA , Ltd.. The 510(k) number is K840225.

When did C-ARM CEILING CRANE FT-2 receive FDA 510(k) clearance?

C-ARM CEILING CRANE FT-2 received FDA 510(k) clearance on 1984-03-22, under 510(k) number K840225.

Who is the listed applicant for C-ARM CEILING CRANE FT-2?

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

What is the FDA product code for C-ARM CEILING CRANE FT-2?

The FDA product code for C-ARM CEILING CRANE FT-2 is JAA.

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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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