FDA 510(k)

MOI-STIR

K-Number: K810157 · 1981-02-10

Decision Date1981-02-10

Product CodeLFD

DecisionSubstantially Equivalent

Device Summary

MOI-STIR is the device name listed in this FDA 510(k) record. The listed applicant is Kingswood Laboratories, Inc.. It received FDA 510(k) clearance on 1981-02-10 under 510(k) number K810157. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOI-STIR?

MOI-STIR is a medical device that received FDA 510(k) clearance on 1981-02-10. The listed applicant is Kingswood Laboratories, Inc.. The 510(k) number is K810157.

When did MOI-STIR receive FDA 510(k) clearance?

MOI-STIR received FDA 510(k) clearance on 1981-02-10, under 510(k) number K810157.

Who is the listed applicant for MOI-STIR?

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

What is the FDA product code for MOI-STIR?

The FDA product code for MOI-STIR is LFD.

Other records listing Kingswood Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K851026MOI-STIR ORAL SWABSTICK(S)K840807THROAT MOI-STIR

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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.