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FDA 510(k)

MULTIPURPOSE DIGITAL GAMMACAMERA, GCA-602A

K-Number: K881013 · 1988-08-29

ApplicantToshiba Medical Systems
Decision Date1988-08-29
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIPURPOSE DIGITAL GAMMACAMERA, GCA-602A 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 1988-08-29 under 510(k) number K881013. 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 MULTIPURPOSE DIGITAL GAMMACAMERA, GCA-602A?

MULTIPURPOSE DIGITAL GAMMACAMERA, GCA-602A is a medical device that received FDA 510(k) clearance on 1988-08-29. The listed applicant is Toshiba Medical Systems. The 510(k) number is K881013.

When did MULTIPURPOSE DIGITAL GAMMACAMERA, GCA-602A receive FDA 510(k) clearance?

MULTIPURPOSE DIGITAL GAMMACAMERA, GCA-602A received FDA 510(k) clearance on 1988-08-29, under 510(k) number K881013.

Who is the listed applicant for MULTIPURPOSE DIGITAL GAMMACAMERA, GCA-602A?

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 MULTIPURPOSE DIGITAL GAMMACAMERA, GCA-602A?

The FDA product code for MULTIPURPOSE DIGITAL GAMMACAMERA, GCA-602A 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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