Charles L. Rose and Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Charles L. Rose and Co., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Charles L. Rose and Co., Inc. has 4 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 4 cleared submissions from 1990 to 1992. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Charles L. Rose and Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Charles L. Rose and Co., Inc.
4 devices
Cleared
Jul 28, 1992
KTP/532 & KTP/YAG SURGICAL LASERS
General & Plastic Surgery
372d
Cleared
Mar 26, 1992
UNISURGE TISSUE COLLECTION SYSTEM FOR ENDOS SURG
General & Plastic Surgery
143d
Cleared
Dec 14, 1990
MODEL GLASE 210 HOLMIUM LASER SYSTEM
Obstetrics & Gynecology
88d
Cleared
Sep 05, 1990
MODEL RD-1200 RUBY LASER SYSTEM
General & Plastic Surgery
15d