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FDA 510(k)

NP15

K-Number: K102515 · 2011-03-11

ApplicantWeinmann Gerate Fur Medizin GmbH + Co. KG
Decision Date2011-03-11
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NP15 is the device name listed in this FDA 510(k) record. The listed applicant is Weinmann Gerate Fur Medizin GmbH + Co. KG. It received FDA 510(k) clearance on 2011-03-11 under 510(k) number K102515. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NP15?

NP15 is a medical device that received FDA 510(k) clearance on 2011-03-11. The listed applicant is Weinmann Gerate Fur Medizin GmbH + Co. KG. The 510(k) number is K102515.

When did NP15 receive FDA 510(k) clearance?

NP15 received FDA 510(k) clearance on 2011-03-11, under 510(k) number K102515.

Who is the listed applicant for NP15?

The FDA 510(k) record lists Weinmann Gerate Fur Medizin GmbH + Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NP15?

The FDA product code for NP15 is BZD.

Other records listing Weinmann Gerate Fur Medizin GmbH + Co. KG as applicant

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Related Devices (Code: BZD)

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

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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