ClearanceBrief
Company ยท US

Laser Media

FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1987. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LNKLaser For Gastro-Urology Use8
HHRLaser, Surgical, Gynecologic2
LLOLaser, Neodymium:Yag, Pulmonary Surgery2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 30, 1987K872352FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA
Laser Media
HHR
Dec 11, 1987K872351FIBERLASE II ND:YAG LASER FOR PULMONARY USE
Laser Media
LLO
Aug 10, 1987K872350FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USE
Laser Media
LNK
Aug 4, 1987K872031UNI-FIBER NON-REPAIRABLE FIBER DELIVERY SYSTEM
Laser Media
LNK
Dec 3, 1986K863428SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAG
Laser Media
LNK
Nov 24, 1986K863583CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER
Laser Media
LNK
Sep 25, 1986K862444FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA
Laser Media
HHR
Feb 5, 1986K860063ND:YAG LASER SINGLE USE FIBER DELIVERY SYSTEM
Laser Media
LNK
Jan 21, 1986K855197FIBERLASE 100 ND: YAG MEDICAL LASER SYSTEM
Laser Media
LNK
Jul 29, 1985K852798FIBERLASE 100 MEDICAL LASER SYSTEM
Laser Media
LNK
Apr 8, 1985K850509ND:YAG FIBERLASE 100 MEDICAL LASER SYSTEM
Laser Media
LNK
Jan 14, 1985K844869FIBERLASE 100 MEDICAL LASER SYSTEM
Laser Media
LLO

Latest recalls

DateFirm and productCodeLinked 510(k)
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