ClearanceBrief
Company ยท US

Lasermatic, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1991. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEXPowered Laser Surgical Instrument5
LNKLaser For Gastro-Urology Use2
EWGLaser, Ent Microsurgical Carbon-Dioxide1
HHRLaser, Surgical, Gynecologic1
LLOLaser, Neodymium:Yag, Pulmonary Surgery1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 19, 1991K903131LASERMATIC SUPERCOMBO(TM) SURGICAL LASER SYSTEM
Lasermatic, Inc.
GEX
Jun 27, 1990K901638MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33
Lasermatic, Inc.
GEX
Nov 8, 1989K895279LASERMATIC COMBOLASER MODEL 5050
Lasermatic OY
GEX
Jun 8, 1989K893529COMBOLASER MODEL 5050
Lasermatic, Inc.
GEX
Aug 22, 1988K871875MODEL 5050 SURGILASER FOR OB-GYN USE
Lasermatic, Inc.
HHR
Aug 10, 1988K870587LASERMATIC SURGILASER MODEL 5050
Lasermatic OY, FI
EWG
Mar 25, 1988K871934MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE
Lasermatic, Inc.
LNK
Mar 25, 1988K871932MODEL 5050 SURGILASER FOR UROLOGY USE
Lasermatic, Inc.
LNK
Jan 22, 1988K871933MODEL 5050 SURGILASER FOR NEUROSURGERY USE
Lasermatic, Inc.
GEX
Jan 22, 1988K871876MODEL 5050 SURGILASER FOR PULMONARY USE
Lasermatic, Inc.
LLO

Latest recalls

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