Medical Device Manufacturer · US , Miami , FL

Leisegang Medical, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1986

Total

Cleared

Denied

Leisegang Medical, Inc. has 10 FDA 510(k) cleared medical devices. Based in Miami, US.

Historical record: 10 cleared submissions from 1986 to 1999. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Leisegang Medical, Inc. Filter by specialty or product code using the sidebar.

Leisegang Medical, 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 - Leisegang Medical, Inc.

10 devices

1-10 of 10

Cleared Feb 11, 1999

SMOOTHLASE ALEXANDRITE LASER SYSTEM

K990043 · GEX

General & Plastic Surgery · 36d

Cleared Apr 25, 1995

COLPOSCOPES AND ACCESSORIES

K940094 · HEX

Obstetrics & Gynecology · 473d

Cleared Jul 02, 1993

LEISEGANG LAPAROSCOPIC IRRIGATION SYSTEM/ACCESS

K924134 · GCS

Gastroenterology & Urology · 318d

Cleared Jul 23, 1992

MAX-E-VAC

K920217 · GEI

General & Plastic Surgery · 189d

Cleared Jan 09, 1992

LM- LAP 10 HIGH FLOW INSUFFLATOR

K914201 · HIF

Obstetrics & Gynecology · 112d

Cleared Sep 20, 1991

LM-100/200LOW FLOW INSUFFLATOR

K912789 · HIG

Obstetrics & Gynecology · 87d

Cleared Sep 18, 1991

LM-300TWIN

K913135 · FSW

General & Plastic Surgery · 64d

Cleared May 23, 1991

LM-150HT LIGHT SOURCE

K911212 · ESI

Ear, Nose, Throat · 65d

Cleared Sep 04, 1990

LM-1Z ZOOM SCOPE

K902313 · HEX

Obstetrics & Gynecology · 104d

Cleared Jan 24, 1986

LM 1000

K854767 · GEH

General & Plastic Surgery · 58d

Leisegang Medical, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Leisegang Medical, Inc.

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