Lca, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lca, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Lca, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Mountain View, US.
Historical record: 12 cleared submissions from 1990 to 1995.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lca, Inc.
12 devices
Cleared
Aug 28, 1995
PADLESS ELECTROSURGICAL PENCIL
General & Plastic Surgery
70d
Cleared
Oct 07, 1994
THE HOOK-CURVED CLOSED END/ELECT FIBER LASER DELIV SYS
General & Plastic Surgery
46d
Cleared
Mar 07, 1994
SNJ SMOKE EVACUATION SUCTION WAND
General Hospital
115d
Cleared
Jan 13, 1994
HYBRID SURGICAL DEVICE MODIFICATION
General & Plastic Surgery
73d
Cleared
Nov 22, 1993
ALLOY SCALPEL HANDPIECES, MODIFICATION
General & Plastic Surgery
374d
Cleared
Oct 05, 1993
CLOSED END FIBEROPTIC LASER DELIVERY SYSTEM
General & Plastic Surgery
217d
Cleared
Apr 23, 1993
HYBRID SURGICAL DEVICE
General & Plastic Surgery
247d
Cleared
Mar 31, 1993
ZOE LASER, CONTACT ND:YAG LASER SYSTEM
General & Plastic Surgery
233d
Cleared
Mar 19, 1993
MOLDED FIBER CAP DELIVERY SYSTEM
General & Plastic Surgery
217d
Cleared
Aug 21, 1990
LASER FORCEPS HANDPIECE
General & Plastic Surgery
151d
Cleared
Jun 20, 1990
REVISED LABELING FOR MODEL CL-0PE ND:YAG LASER
General & Plastic Surgery
9d
Cleared
Apr 16, 1990
CL-OPE CONTACT LASER SYSTEM
General & Plastic Surgery
97d