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FDA 510(k)

SONOS 2000, SONOS 2500 (M2406 A)

K-Number: K964309 · 1997-04-22

ApplicantHewlett-Packard Co.
Decision Date1997-04-22
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONOS 2000, SONOS 2500 (M2406 A) 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 1997-04-22 under 510(k) number K964309. 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 2000, SONOS 2500 (M2406 A)?

SONOS 2000, SONOS 2500 (M2406 A) is a medical device that received FDA 510(k) clearance on 1997-04-22. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K964309.

When did SONOS 2000, SONOS 2500 (M2406 A) receive FDA 510(k) clearance?

SONOS 2000, SONOS 2500 (M2406 A) received FDA 510(k) clearance on 1997-04-22, under 510(k) number K964309.

Who is the listed applicant for SONOS 2000, SONOS 2500 (M2406 A)?

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 2000, SONOS 2500 (M2406 A)?

The FDA product code for SONOS 2000, SONOS 2500 (M2406 A) is IYN.

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Related Devices (Code: IYN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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