Company · US

Laserguide

FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 1988. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
GEX	Powered Laser Surgical Instrument	2
FCS	Light, Catheter, Fiberoptic, Glass, Ureteral	1
LLO	Laser, Neodymium:Yag, Pulmonary Surgery	1
LNK	Laser For Gastro-Urology Use	1

Decided	510(k)	Device and applicant	Code
Mar 22, 1988	K880071	SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE Laserguide	FCS
Feb 2, 1988	K875104	SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USE Laserguide	LLO
Feb 2, 1988	K873892	SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE Laserguide	LNK
Nov 6, 1987	K873664	LIGHT-SPOT FIBEROPTIC LASER HANDPIECE Laserguide	GEX
Nov 6, 1987	K873571	LIGHT-TOUCH FIBEROPTIC MICROCONTACT PROBE Laserguide	GEX

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.