Lca, Inc.
FDA 510(k) medical device clearances.
Top product codes for Lca, Inc.
Recent clearances by Lca, Inc.
- K952792 — PADLESS ELECTROSURGICAL PENCIL
- K944091 — THE HOOK-CURVED CLOSED END/ELECT FIBER LASER DELIV SYS
- K935439 — SNJ SMOKE EVACUATION SUCTION WAND
- K935258 — HYBRID SURGICAL DEVICE MODIFICATION
- K925726 — ALLOY SCALPEL HANDPIECES, MODIFICATION
- K931070 — CLOSED END FIBEROPTIC LASER DELIVERY SYSTEM
- K924160 — HYBRID SURGICAL DEVICE
- K923991 — ZOE LASER, CONTACT ND:YAG LASER SYSTEM
- K924120 — MOLDED FIBER CAP DELIVERY SYSTEM
- K901365 — LASER FORCEPS HANDPIECE
- K902562 — REVISED LABELING FOR MODEL CL-0PE ND:YAG LASER
- K900128 — CL-OPE CONTACT LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.