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FDA 510(k)

CAMERA, GCA-10A, LOW ENERGY

K-Number: K781739 · 1978-11-27

ApplicantToshiba Medical Systems
Decision Date1978-11-27
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAMERA, GCA-10A, LOW ENERGY is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems. It received FDA 510(k) clearance on 1978-11-27 under 510(k) number K781739. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMERA, GCA-10A, LOW ENERGY?

CAMERA, GCA-10A, LOW ENERGY is a medical device that received FDA 510(k) clearance on 1978-11-27. The listed applicant is Toshiba Medical Systems. The 510(k) number is K781739.

When did CAMERA, GCA-10A, LOW ENERGY receive FDA 510(k) clearance?

CAMERA, GCA-10A, LOW ENERGY received FDA 510(k) clearance on 1978-11-27, under 510(k) number K781739.

Who is the listed applicant for CAMERA, GCA-10A, LOW ENERGY?

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

What is the FDA product code for CAMERA, GCA-10A, LOW ENERGY?

The FDA product code for CAMERA, GCA-10A, LOW ENERGY is IYX.

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Related Devices (Code: IYX)

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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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