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FDA 510(k)

FLOSIMPLE ARTHROSCOPY PUMP A120

K-Number: K062380 · 2006-12-14

ApplicantW.O.M. World of Medicine AG
Decision Date2006-12-14
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FLOSIMPLE ARTHROSCOPY PUMP A120 is the device name listed in this FDA 510(k) record. The listed applicant is W.O.M. World of Medicine AG. It received FDA 510(k) clearance on 2006-12-14 under 510(k) number K062380. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOSIMPLE ARTHROSCOPY PUMP A120?

FLOSIMPLE ARTHROSCOPY PUMP A120 is a medical device that received FDA 510(k) clearance on 2006-12-14. The listed applicant is W.O.M. World of Medicine AG. The 510(k) number is K062380.

When did FLOSIMPLE ARTHROSCOPY PUMP A120 receive FDA 510(k) clearance?

FLOSIMPLE ARTHROSCOPY PUMP A120 received FDA 510(k) clearance on 2006-12-14, under 510(k) number K062380.

Who is the listed applicant for FLOSIMPLE ARTHROSCOPY PUMP A120?

The FDA 510(k) record lists W.O.M. World of Medicine AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOSIMPLE ARTHROSCOPY PUMP A120?

The FDA product code for FLOSIMPLE ARTHROSCOPY PUMP A120 is HRX.

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Related Devices (Code: HRX)

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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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