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FDA 510(k)

JUMBO DIGITAL GAMMACAMERA, GCA-901A

K-Number: K871175 · 1987-03-31

ApplicantToshiba Medical Systems
Decision Date1987-03-31
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

JUMBO DIGITAL GAMMACAMERA, GCA-901A 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 1987-03-31 under 510(k) number K871175. 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 JUMBO DIGITAL GAMMACAMERA, GCA-901A?

JUMBO DIGITAL GAMMACAMERA, GCA-901A is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Toshiba Medical Systems. The 510(k) number is K871175.

When did JUMBO DIGITAL GAMMACAMERA, GCA-901A receive FDA 510(k) clearance?

JUMBO DIGITAL GAMMACAMERA, GCA-901A received FDA 510(k) clearance on 1987-03-31, under 510(k) number K871175.

Who is the listed applicant for JUMBO DIGITAL GAMMACAMERA, GCA-901A?

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 JUMBO DIGITAL GAMMACAMERA, GCA-901A?

The FDA product code for JUMBO DIGITAL GAMMACAMERA, GCA-901A 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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