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FDA 510(k)

THROAT MOI-STIR

K-Number: K840807 · 1984-05-25

ApplicantKingswood Laboratories, Inc.
Decision Date1984-05-25
Product CodeLFD
DecisionSubstantially Equivalent

Device Summary

THROAT 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 1984-05-25 under 510(k) number K840807. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THROAT MOI-STIR?

THROAT MOI-STIR is a medical device that received FDA 510(k) clearance on 1984-05-25. The listed applicant is Kingswood Laboratories, Inc.. The 510(k) number is K840807.

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

THROAT MOI-STIR received FDA 510(k) clearance on 1984-05-25, under 510(k) number K840807.

Who is the listed applicant for THROAT 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 THROAT MOI-STIR?

The FDA product code for THROAT MOI-STIR is LFD.

Related Clinical Trials

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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)K810157MOI-STIR

Related Devices (Code: LFD)

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.

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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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