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FDA 510(k)

RUGALIFT, MODEL# V.2.1

K-Number: K071573 · 2008-12-09

ApplicantFatrotek S.R.L.
Decision Date2008-12-09
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RUGALIFT, MODEL# V.2.1 is the device name listed in this FDA 510(k) record. The listed applicant is Fatrotek S.R.L.. It received FDA 510(k) clearance on 2008-12-09 under 510(k) number K071573. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUGALIFT, MODEL# V.2.1?

RUGALIFT, MODEL# V.2.1 is a medical device that received FDA 510(k) clearance on 2008-12-09. The listed applicant is Fatrotek S.R.L.. The 510(k) number is K071573.

When did RUGALIFT, MODEL# V.2.1 receive FDA 510(k) clearance?

RUGALIFT, MODEL# V.2.1 received FDA 510(k) clearance on 2008-12-09, under 510(k) number K071573.

Who is the listed applicant for RUGALIFT, MODEL# V.2.1?

The FDA 510(k) record lists Fatrotek S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RUGALIFT, MODEL# V.2.1?

The FDA product code for RUGALIFT, MODEL# V.2.1 is NFO.

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Related Devices (Code: NFO)

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

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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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