Medical Device Manufacturer · US , Mchenry , IL

Aspen Laboratories, Inc. - FDA 510(k) Cleared Devices

55 submissions · 55 cleared · Since 1976

Total

Cleared

Denied

Aspen Laboratories, Inc. has 55 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 55 cleared submissions from 1976 to 1998. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Aspen Laboratories, Inc.

55 devices

1-12 of 55

Cleared Apr 21, 1998

SYSTEM 7500 ABC ELECTROSURGICAL UNIT

K981220 · GEI

General & Plastic Surgery · 18d

Cleared Sep 13, 1996

SHEATH, ELECTROSURGICAL PENCIL

K963088 · GEI

General & Plastic Surgery · 36d

Cleared Jul 11, 1996

SYSTEM 6500 ABC ELECTROSURGICAL UNIT

K955834 · GEI

General & Plastic Surgery · 198d

Cleared Feb 20, 1996

4000 ETM

K960296 · GEI

General & Plastic Surgery · 29d

Cleared Oct 30, 1995

BEAMER PLUS

K953081 · GEI

General & Plastic Surgery · 119d

Cleared Aug 21, 1995

EXCALIBUR PLUS ELECTROSURGICAL UNIT

K953007 · GEI

General & Plastic Surgery · 54d

Cleared Apr 03, 1995

SMOKIEVAC ELECTROSURGICAL PENCIL

K946104 · GEI

General & Plastic Surgery · 110d

Cleared Dec 21, 1994

ELECTROSURGICAL FLEXIBLE ELECTRODE IN-LINE SUCTION COAGULATOR

K944012 · GEI

General & Plastic Surgery · 127d

Cleared Apr 16, 1993

EXCALIBUR ELECTROSURGICAL UNIT

K924960 · GEI

General & Plastic Surgery · 198d

Cleared Feb 13, 1992

SINGLE USE LEE ELECTRODE

K913213 · HGI

Obstetrics & Gynecology · 209d

Cleared Feb 13, 1990

BISTAT ELECTROSURGICAL UNIT 60-5400-001

K896838 · GEX

General & Plastic Surgery · 70d

Cleared Feb 02, 1990

MF-450 ELECTROSURGICAL UNIT 60-5500-001

K896839 · GEI

General & Plastic Surgery · 59d

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Aspen Laboratories, Inc. - FDA 510(k) Cleared Devices

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