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FDA 510(k)

OMNISTICK

K-Number: K830310 · 1983-05-25

ApplicantMarquest Medical Products, Inc.
Decision Date1983-05-25
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OMNISTICK 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 1983-05-25 under 510(k) number K830310. 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 OMNISTICK?

OMNISTICK is a medical device that received FDA 510(k) clearance on 1983-05-25. The listed applicant is Marquest Medical Products, Inc.. The 510(k) number is K830310.

When did OMNISTICK receive FDA 510(k) clearance?

OMNISTICK received FDA 510(k) clearance on 1983-05-25, under 510(k) number K830310.

Who is the listed applicant for OMNISTICK?

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 OMNISTICK?

The FDA product code for OMNISTICK is CBT.

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Other records listing Marquest Medical Products, Inc. as applicant

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Related Devices (Code: 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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