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FDA 510(k)

UNIX-LINK

K-Number: K926550 · 1993-03-18

ApplicantGeneral Electric Co.
Decision Date1993-03-18
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UNIX-LINK 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 1993-03-18 under 510(k) number K926550. 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 UNIX-LINK?

UNIX-LINK is a medical device that received FDA 510(k) clearance on 1993-03-18. The listed applicant is General Electric Co.. The 510(k) number is K926550.

When did UNIX-LINK receive FDA 510(k) clearance?

UNIX-LINK received FDA 510(k) clearance on 1993-03-18, under 510(k) number K926550.

Who is the listed applicant for UNIX-LINK?

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 UNIX-LINK?

The FDA product code for UNIX-LINK 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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