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FDA 510(k)

STUMARK INFUSOR

K-Number: K810252 · 1981-03-17

ApplicantStumark Corp.
Decision Date1981-03-17
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STUMARK INFUSOR is the device name listed in this FDA 510(k) record. The listed applicant is Stumark Corp.. It received FDA 510(k) clearance on 1981-03-17 under 510(k) number K810252. 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 STUMARK INFUSOR?

STUMARK INFUSOR is a medical device that received FDA 510(k) clearance on 1981-03-17. The listed applicant is Stumark Corp.. The 510(k) number is K810252.

When did STUMARK INFUSOR receive FDA 510(k) clearance?

STUMARK INFUSOR received FDA 510(k) clearance on 1981-03-17, under 510(k) number K810252.

Who is the listed applicant for STUMARK INFUSOR?

The FDA 510(k) record lists Stumark Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STUMARK INFUSOR?

The FDA product code for STUMARK INFUSOR is FRN.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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