Medical Device Manufacturer · US , Chicago , IL

L.A.S.E.R., Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1985

Total

Cleared

Denied

L.A.S.E.R., Inc. has 14 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 14 cleared submissions from 1985 to 1998. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by L.A.S.E.R., Inc. Filter by specialty or product code using the sidebar.

L.A.S.E.R., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - L.A.S.E.R., Inc.

14 devices

1-12 of 14

Cleared Dec 22, 1998

CO2 LASER COUPLER

K983965 · GEX

General & Plastic Surgery · 46d

Cleared Mar 31, 1995

REUSABLE TROCAR WITH SAFETY SLEEVE

K950021 · GCJ

General & Plastic Surgery · 86d

Cleared Mar 25, 1994

GRASPING FORCEPS, PUNCHES, SCISSORS

Obstetrics & Gynecology · 314d

Cleared Nov 02, 1993

ENDOSCOPIC INSTRUMENTS AND ACCESSDORIES

K933421 · GCJ

General & Plastic Surgery · 112d

Cleared Oct 08, 1993

BULK TISSUE REMOVAL SYSTEM

K924844 · HET

Obstetrics & Gynecology · 375d

Cleared Sep 23, 1993

DISPOSABLE INSUFFLATION TUBING

K932045 · GCJ

General & Plastic Surgery · 149d

Cleared Apr 30, 1993

ENDOSCOPIC RETRACTOR

K931092 · GCJ

General & Plastic Surgery · 58d

Cleared Apr 10, 1992

ALLOY SCALPEL HANDPIECES

K914197 · GEX

General & Plastic Surgery · 204d

Cleared Feb 21, 1991

TROCAR DISPOSABLE

K904638 · FBQ

General & Plastic Surgery · 133d

Cleared Mar 06, 1990

MODEL JM-1 CO2 LASER

K892912 · GEX

General & Plastic Surgery · 320d

Cleared Oct 16, 1985

DOUBLE PUNCTURE INSTRUMENTS

K852901 · HET

Obstetrics & Gynecology · 99d

L.A.S.E.R., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - L.A.S.E.R., Inc.

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