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FDA 510(k)

AUTO STIK

K-Number: K830311 · 1983-05-25

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

Device Summary

AUTO STIK 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 K830311. 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 AUTO STIK?

AUTO STIK 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 K830311.

When did AUTO STIK receive FDA 510(k) clearance?

AUTO STIK received FDA 510(k) clearance on 1983-05-25, under 510(k) number K830311.

Who is the listed applicant for AUTO STIK?

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 AUTO STIK?

The FDA product code for AUTO STIK 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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