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FDA 510(k)

MOI-STIR ORAL SWABSTICK(S)

K-Number: K851026 · 1985-05-21

ApplicantKingswood Laboratories, Inc.
Decision Date1985-05-21
Product CodeLFD
DecisionSubstantially Equivalent

Device Summary

MOI-STIR ORAL SWABSTICK(S) 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 1985-05-21 under 510(k) number K851026. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOI-STIR ORAL SWABSTICK(S)?

MOI-STIR ORAL SWABSTICK(S) is a medical device that received FDA 510(k) clearance on 1985-05-21. The listed applicant is Kingswood Laboratories, Inc.. The 510(k) number is K851026.

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

MOI-STIR ORAL SWABSTICK(S) received FDA 510(k) clearance on 1985-05-21, under 510(k) number K851026.

Who is the listed applicant for MOI-STIR ORAL SWABSTICK(S)?

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 ORAL SWABSTICK(S)?

The FDA product code for MOI-STIR ORAL SWABSTICK(S) 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.

K840807THROAT MOI-STIRK810157MOI-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

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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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