Medical Device Manufacturer · US , Albuquerque , NM

Cell Robotics, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1997

Recent clearances: LASETTE, CELL ROBOTICS' LASETTE, LASETTE LASER SKIN PERFORATOR

Total

Cleared

Denied

Cell Robotics, Inc. has 9 FDA 510(k) cleared medical devices. Based in Albuquerque, US.

Historical record: 9 cleared submissions from 1997 to 2003. Primary specialty: General & Plastic Surgery.

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

Cell Robotics, Inc. is one of 8094 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cell Robotics, Inc.

9 devices

1-9 of 9

Cleared Dec 22, 2003

CLINICAL LASETTE P-200

K033799 · GEX

General & Plastic Surgery · 17d

Cleared Sep 11, 2002

CELL ROBOTICS ULTRA-LIGHT PEEL LASER SYSTEM

K021946 · GEX

General & Plastic Surgery · 90d

Cleared Jan 15, 1999

LASETTE

K983673 · GEX

General & Plastic Surgery · 87d

Cleared Dec 07, 1998

CELL ROBOTICS' LASETTE

K981746 · GEX

General & Plastic Surgery · 203d

Cleared Sep 24, 1998

LASETTE LASER SKIN PERFORATOR

K982230 · GEX

General & Plastic Surgery · 177d

Cleared Jun 29, 1998

LASETTE LASER SKIN PERFORATOR

K981149 · GEX

General & Plastic Surgery · 90d

Cleared Oct 28, 1997

LASETTE

K973431 · GEX

General & Plastic Surgery · 48d

Cleared Aug 14, 1997

LASETTE

K965124 · GEX

General & Plastic Surgery · 234d

Cleared Jul 11, 1997

CELL ROBOTICS ER: YAG SURGICAL LASER

K970461 · GEX

General & Plastic Surgery · 155d

Cell Robotics, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Cell Robotics, Inc.

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