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FDA 510(k)

STERI-SWAB

K-Number: K912731 · 1991-10-02

ApplicantWestlock Investments (Usa), Inc.
Decision Date1991-10-02
Product CodeLKB
DecisionSubstantially Equivalent

Device Summary

STERI-SWAB is the device name listed in this FDA 510(k) record. The listed applicant is Westlock Investments (Usa), Inc.. It received FDA 510(k) clearance on 1991-10-02 under 510(k) number K912731. The device is classified under product code LKB. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERI-SWAB?

STERI-SWAB is a medical device that received FDA 510(k) clearance on 1991-10-02. The listed applicant is Westlock Investments (Usa), Inc.. The 510(k) number is K912731.

When did STERI-SWAB receive FDA 510(k) clearance?

STERI-SWAB received FDA 510(k) clearance on 1991-10-02, under 510(k) number K912731.

Who is the listed applicant for STERI-SWAB?

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

What is the FDA product code for STERI-SWAB?

The FDA product code for STERI-SWAB is LKB.

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Related Devices (Code: LKB)

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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