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FDA 510(k)

VSPSPN

K-Number: K063438 · 2007-01-17

ApplicantTecres S.P.A.
Decision Date2007-01-17
Product CodeNDN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VSPSPN is the device name listed in this FDA 510(k) record. The listed applicant is Tecres S.P.A.. It received FDA 510(k) clearance on 2007-01-17 under 510(k) number K063438. The device is classified under product code NDN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VSPSPN?

VSPSPN is a medical device that received FDA 510(k) clearance on 2007-01-17. The listed applicant is Tecres S.P.A.. The 510(k) number is K063438.

When did VSPSPN receive FDA 510(k) clearance?

VSPSPN received FDA 510(k) clearance on 2007-01-17, under 510(k) number K063438.

Who is the listed applicant for VSPSPN?

The FDA 510(k) record lists Tecres S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VSPSPN?

The FDA product code for VSPSPN is NDN.

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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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