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FDA 510(k)

QUEST 521 VARIABLE PRESSURE VOLUMETRIC INFUSION PU

K-Number: K851017 · 1985-05-07

ApplicantQuest Medical, Inc.
Decision Date1985-05-07
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

QUEST 521 VARIABLE PRESSURE VOLUMETRIC INFUSION PU 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 1985-05-07 under 510(k) number K851017. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUEST 521 VARIABLE PRESSURE VOLUMETRIC INFUSION PU?

QUEST 521 VARIABLE PRESSURE VOLUMETRIC INFUSION PU is a medical device that received FDA 510(k) clearance on 1985-05-07. The listed applicant is Quest Medical, Inc.. The 510(k) number is K851017.

When did QUEST 521 VARIABLE PRESSURE VOLUMETRIC INFUSION PU receive FDA 510(k) clearance?

QUEST 521 VARIABLE PRESSURE VOLUMETRIC INFUSION PU received FDA 510(k) clearance on 1985-05-07, under 510(k) number K851017.

Who is the listed applicant for QUEST 521 VARIABLE PRESSURE VOLUMETRIC INFUSION PU?

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 521 VARIABLE PRESSURE VOLUMETRIC INFUSION PU?

The FDA product code for QUEST 521 VARIABLE PRESSURE VOLUMETRIC INFUSION PU is FRN.

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Related Devices (Code: FRN)

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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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