LC COMPOSITE
K-Number: K991492 · 1999-12-02
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Device Summary
Frequently Asked Questions
What is the LC COMPOSITE?
LC COMPOSITE is a medical device that received FDA 510(k) clearance on 1999-12-02. The listed applicant is Harry J. Bosworth Co.. The 510(k) number is K991492.
When did LC COMPOSITE receive FDA 510(k) clearance?
LC COMPOSITE received FDA 510(k) clearance on 1999-12-02, under 510(k) number K991492.
Who is the listed applicant for LC COMPOSITE?
The FDA 510(k) record lists Harry J. Bosworth Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LC COMPOSITE?
The FDA product code for LC COMPOSITE is EFB.
Related Clinical Trials
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.
Other records listing Harry J. Bosworth Co. 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.
Related Devices (Code: EFB)
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.
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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