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FDA 510(k)

VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22

K-Number: K993907 · 1999-12-06

ApplicantAgilent Technologies, Inc.
Decision Date1999-12-06
Product CodeMHD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22 is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies, Inc.. It received FDA 510(k) clearance on 1999-12-06 under 510(k) number K993907. The device is classified under product code MHD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22?

VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22 is a medical device that received FDA 510(k) clearance on 1999-12-06. The listed applicant is Agilent Technologies, Inc.. The 510(k) number is K993907.

When did VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22 receive FDA 510(k) clearance?

VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22 received FDA 510(k) clearance on 1999-12-06, under 510(k) number K993907.

Who is the listed applicant for VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22?

The FDA 510(k) record lists Agilent Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22?

The FDA product code for VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22 is MHD.

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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.

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