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FDA 510(k)

TENSCARE ULTIMA NMS/EMS

K-Number: K023997 · 2003-03-03

ApplicantTenscare, Ltd.
Decision Date2003-03-03
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TENSCARE ULTIMA NMS/EMS is the device name listed in this FDA 510(k) record. The listed applicant is Tenscare, Ltd.. It received FDA 510(k) clearance on 2003-03-03 under 510(k) number K023997. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENSCARE ULTIMA NMS/EMS?

TENSCARE ULTIMA NMS/EMS is a medical device that received FDA 510(k) clearance on 2003-03-03. The listed applicant is Tenscare, Ltd.. The 510(k) number is K023997.

When did TENSCARE ULTIMA NMS/EMS receive FDA 510(k) clearance?

TENSCARE ULTIMA NMS/EMS received FDA 510(k) clearance on 2003-03-03, under 510(k) number K023997.

Who is the listed applicant for TENSCARE ULTIMA NMS/EMS?

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

What is the FDA product code for TENSCARE ULTIMA NMS/EMS?

The FDA product code for TENSCARE ULTIMA NMS/EMS is IPF.

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Related Devices (Code: IPF)

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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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