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FDA 510(k)

NHAC 16

K-Number: K171515 · 2017-07-26

ApplicantLmt Medical Systems GmbH
Decision Date2017-07-26
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NHAC 16 is the device name listed in this FDA 510(k) record. The listed applicant is Lmt Medical Systems GmbH. It received FDA 510(k) clearance on 2017-07-26 under 510(k) number K171515. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NHAC 16?

NHAC 16 is a medical device that received FDA 510(k) clearance on 2017-07-26. The listed applicant is Lmt Medical Systems GmbH. The 510(k) number is K171515.

When did NHAC 16 receive FDA 510(k) clearance?

NHAC 16 received FDA 510(k) clearance on 2017-07-26, under 510(k) number K171515.

Who is the listed applicant for NHAC 16?

The FDA 510(k) record lists Lmt Medical Systems GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NHAC 16?

The FDA product code for NHAC 16 is MOS.

Related Devices (Code: MOS)

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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