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FDA 510(k)

OMNISTIK, MQ 501GS

K-Number: K800860 · 1980-04-29

ApplicantMarquest Medical Products, Inc.
Decision Date1980-04-29
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OMNISTIK, MQ 501GS is the device name listed in this FDA 510(k) record. The listed applicant is Marquest Medical Products, Inc.. It received FDA 510(k) clearance on 1980-04-29 under 510(k) number K800860. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNISTIK, MQ 501GS?

OMNISTIK, MQ 501GS is a medical device that received FDA 510(k) clearance on 1980-04-29. The listed applicant is Marquest Medical Products, Inc.. The 510(k) number is K800860.

When did OMNISTIK, MQ 501GS receive FDA 510(k) clearance?

OMNISTIK, MQ 501GS received FDA 510(k) clearance on 1980-04-29, under 510(k) number K800860.

Who is the listed applicant for OMNISTIK, MQ 501GS?

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

What is the FDA product code for OMNISTIK, MQ 501GS?

The FDA product code for OMNISTIK, MQ 501GS is CBT.

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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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