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FDA 510(k)

QUEST MPS BACK-UP SYSYEM

K-Number: K002366 · 2000-09-18

ApplicantQuest Medical, Inc.
Decision Date2000-09-18
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUEST MPS BACK-UP SYSYEM is the device name listed in this FDA 510(k) record. The listed applicant is Quest Medical, Inc.. It received FDA 510(k) clearance on 2000-09-18 under 510(k) number K002366. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUEST MPS BACK-UP SYSYEM?

QUEST MPS BACK-UP SYSYEM is a medical device that received FDA 510(k) clearance on 2000-09-18. The listed applicant is Quest Medical, Inc.. The 510(k) number is K002366.

When did QUEST MPS BACK-UP SYSYEM receive FDA 510(k) clearance?

QUEST MPS BACK-UP SYSYEM received FDA 510(k) clearance on 2000-09-18, under 510(k) number K002366.

Who is the listed applicant for QUEST MPS BACK-UP SYSYEM?

The FDA 510(k) record lists Quest Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUEST MPS BACK-UP SYSYEM?

The FDA product code for QUEST MPS BACK-UP SYSYEM is DWF.

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Related Devices (Code: DWF)

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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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