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FDA 510(k)

DISPENSER DP 20

K-Number: K071588 · 2007-11-26

ApplicantNOUVAG AG
Decision Date2007-11-26
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPENSER DP 20 is the device name listed in this FDA 510(k) record. The listed applicant is NOUVAG AG. It received FDA 510(k) clearance on 2007-11-26 under 510(k) number K071588. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPENSER DP 20?

DISPENSER DP 20 is a medical device that received FDA 510(k) clearance on 2007-11-26. The listed applicant is NOUVAG AG. The 510(k) number is K071588.

When did DISPENSER DP 20 receive FDA 510(k) clearance?

DISPENSER DP 20 received FDA 510(k) clearance on 2007-11-26, under 510(k) number K071588.

Who is the listed applicant for DISPENSER DP 20?

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

What is the FDA product code for DISPENSER DP 20?

The FDA product code for DISPENSER DP 20 is FRN.

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Other records listing NOUVAG AG as applicant

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Related Devices (Code: FRN)

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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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