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FDA 510(k)

COMPUTED TOMOGRAPHY ORIENTED ROTARY ARC

K-Number: K833484 · 1983-12-29

ApplicantA. Patil, M.D.
Decision Date1983-12-29
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

COMPUTED TOMOGRAPHY ORIENTED ROTARY ARC is the device name listed in this FDA 510(k) record. The listed applicant is A. Patil, M.D.. It received FDA 510(k) clearance on 1983-12-29 under 510(k) number K833484. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPUTED TOMOGRAPHY ORIENTED ROTARY ARC?

COMPUTED TOMOGRAPHY ORIENTED ROTARY ARC is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is A. Patil, M.D.. The 510(k) number is K833484.

When did COMPUTED TOMOGRAPHY ORIENTED ROTARY ARC receive FDA 510(k) clearance?

COMPUTED TOMOGRAPHY ORIENTED ROTARY ARC received FDA 510(k) clearance on 1983-12-29, under 510(k) number K833484.

Who is the listed applicant for COMPUTED TOMOGRAPHY ORIENTED ROTARY ARC?

The FDA 510(k) record lists A. Patil, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPUTED TOMOGRAPHY ORIENTED ROTARY ARC?

The FDA product code for COMPUTED TOMOGRAPHY ORIENTED ROTARY ARC is HAW.

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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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