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FDA 510(k)

STRUVA & MEDI

K-Number: K811173 · 1981-06-18

ApplicantWeco
Decision Date1981-06-18
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRUVA & MEDI is the device name listed in this FDA 510(k) record. The listed applicant is Weco. It received FDA 510(k) clearance on 1981-06-18 under 510(k) number K811173. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRUVA & MEDI?

STRUVA & MEDI is a medical device that received FDA 510(k) clearance on 1981-06-18. The listed applicant is Weco. The 510(k) number is K811173.

When did STRUVA & MEDI receive FDA 510(k) clearance?

STRUVA & MEDI received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811173.

Who is the listed applicant for STRUVA & MEDI?

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

What is the FDA product code for STRUVA & MEDI?

The FDA product code for STRUVA & MEDI is FQM.

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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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