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FDA 510(k)

Möller Medical Biopsy Needles and Systems

K-Number: K162588 · 2017-06-19

ApplicantMoller Medical GmbH
Decision Date2017-06-19
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Möller Medical Biopsy Needles and Systems is a medical device manufactured by Moller Medical GmbH. It received FDA 510(k) clearance on 2017-06-19 under approval number K162588. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Möller Medical Biopsy Needles and Systems?

Möller Medical Biopsy Needles and Systems is a medical device that received FDA 510(k) clearance on 2017-06-19. It is manufactured by Moller Medical GmbH. The 510(k) number is K162588.

When was Möller Medical Biopsy Needles and Systems approved by the FDA?

Möller Medical Biopsy Needles and Systems received FDA 510(k) clearance on 2017-06-19, under approval number K162588.

What company makes Möller Medical Biopsy Needles and Systems?

Möller Medical Biopsy Needles and Systems is manufactured by Moller Medical GmbH.

What is the FDA product code for Möller Medical Biopsy Needles and Systems?

The FDA product code for Möller Medical Biopsy Needles and Systems is KNW.

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Related Devices (Code: KNW)

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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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