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FDA 510(k)

MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM

K-Number: K092387 · 2010-04-05

ApplicantMinntech Corp.
Decision Date2010-04-05
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Minntech Corp.. It received FDA 510(k) clearance on 2010-04-05 under 510(k) number K092387. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM?

MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM is a medical device that received FDA 510(k) clearance on 2010-04-05. The listed applicant is Minntech Corp.. The 510(k) number is K092387.

When did MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM receive FDA 510(k) clearance?

MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM received FDA 510(k) clearance on 2010-04-05, under 510(k) number K092387.

Who is the listed applicant for MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM?

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

What is the FDA product code for MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM?

The FDA product code for MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM is FEB.

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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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