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FDA 510(k)

P-3 CLOSING INSTRUMENT

K-Number: K850041 · 1985-02-21

ApplicantLone Star Medical Products, Inc.
Decision Date1985-02-21
Product Code
DecisionSubstantially Equivalent

Device Summary

P-3 CLOSING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Lone Star Medical Products, Inc.. It received FDA 510(k) clearance on 1985-02-21 under 510(k) number K850041. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P-3 CLOSING INSTRUMENT?

P-3 CLOSING INSTRUMENT is a medical device that received FDA 510(k) clearance on 1985-02-21. The listed applicant is Lone Star Medical Products, Inc.. The 510(k) number is K850041.

When did P-3 CLOSING INSTRUMENT receive FDA 510(k) clearance?

P-3 CLOSING INSTRUMENT received FDA 510(k) clearance on 1985-02-21, under 510(k) number K850041.

Who is the listed applicant for P-3 CLOSING INSTRUMENT?

The FDA 510(k) record lists Lone Star Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Lone Star Medical Products, 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.

K831531SURGICAL ISOLATION BARRIER SYSTEMK820015URETHAL CUTTER CLAMPK810915THE SCOTT DIALMENZENSERTK802983THE INQUINAL RESORVOIR INSERTERK791665SCOTTS SURGICAL RETRACTOR AND ELASTIC

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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