K850041Substantially Equivalent

P-3 Closing Instrument

Name: K850041 P-3 Closing Instrument
Creator: Lone Star Medical Products, Inc.
Published: 1985-02-21
License: https://open.fda.gov/license/

Lone Star Medical Products, Houston TX / Traditional, Substantially Equivalent

FDA source

K850041 is the FDA 510(k) clearance record for P-3 CLOSING INSTRUMENT, cleared for Lone Star Medical Products, Inc. on 1985-02-21. FDA records list 6 510(k) clearances for Lone Star Medical Products, Inc., from 1979-09-19 to 1985-02-21. As of 2026-09-10, FDA records show no recalls naming K850041.

Clearance record

Decision date: 1985-02-21
Received: 1985-01-07 (45 days to decision)
Review panel: Unknown
Applicant: Lone Star Medical Products, Inc. P.O. Box 20701, Houston TX
Third party review: No