FDA 510(k)

VSI 1000

K-Number: K912921 · 1992-10-30

Decision Date1992-10-30

Product CodeFMT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VSI 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Vitaltrends Technology, Inc.. It received FDA 510(k) clearance on 1992-10-30 under 510(k) number K912921. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VSI 1000?

VSI 1000 is a medical device that received FDA 510(k) clearance on 1992-10-30. The listed applicant is Vitaltrends Technology, Inc.. The 510(k) number is K912921.

When did VSI 1000 receive FDA 510(k) clearance?

VSI 1000 received FDA 510(k) clearance on 1992-10-30, under 510(k) number K912921.

Who is the listed applicant for VSI 1000?

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

What is the FDA product code for VSI 1000?

The FDA product code for VSI 1000 is FMT.

Related Devices (Code: FMT)

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.

K243606Babyroo TN300Draeger Medical Systems, Inc.K230278Babyroo TN300Draeger Medical Systems, Inc.K213551Giraffe Omnibed Carestation CS1Datex Ohmeda, Inc.K201628Panda iRes Warmer, Giraffe WarmerGE Healthcare K200319HYDRO-TEMP Neonatal Skin Surface Temperature Sensor, HYDRO-TEMP Neonatal Skin Surface Temperature Sensor with Interface CableDeroyal Industries, Inc.K191425Hydro-Temp Neonatal Skin Temperature Probe CoverDeroyal Industries, Inc.

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.