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FDA 510(k)

ARRANGE TM

K-Number: K820688 · 1982-03-31

ApplicantGeneral Electric Co.
Decision Date1982-03-31
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARRANGE TM is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1982-03-31 under 510(k) number K820688. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARRANGE TM?

ARRANGE TM is a medical device that received FDA 510(k) clearance on 1982-03-31. The listed applicant is General Electric Co.. The 510(k) number is K820688.

When did ARRANGE TM receive FDA 510(k) clearance?

ARRANGE TM received FDA 510(k) clearance on 1982-03-31, under 510(k) number K820688.

Who is the listed applicant for ARRANGE TM?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARRANGE TM?

The FDA product code for ARRANGE TM is JAK.

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Related Devices (Code: JAK)

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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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