FDA 510(k)

SONOS 5500 IMAGING SYSTEM M2424A VERSION B.O

K-Number: K990339 · 1999-02-18

Decision Date1999-02-18

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SONOS 5500 IMAGING SYSTEM M2424A VERSION B.O is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1999-02-18 under 510(k) number K990339. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONOS 5500 IMAGING SYSTEM M2424A VERSION B.O?

SONOS 5500 IMAGING SYSTEM M2424A VERSION B.O is a medical device that received FDA 510(k) clearance on 1999-02-18. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K990339.

When did SONOS 5500 IMAGING SYSTEM M2424A VERSION B.O receive FDA 510(k) clearance?

SONOS 5500 IMAGING SYSTEM M2424A VERSION B.O received FDA 510(k) clearance on 1999-02-18, under 510(k) number K990339.

Who is the listed applicant for SONOS 5500 IMAGING SYSTEM M2424A VERSION B.O?

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

What is the FDA product code for SONOS 5500 IMAGING SYSTEM M2424A VERSION B.O?

The FDA product code for SONOS 5500 IMAGING SYSTEM M2424A VERSION B.O is IYN.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.