Medical Device Manufacturer · US , Palo Alto , CA

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

6 submissions · 6 cleared · Since 1996

Recent clearances: INDIGO PROSTATE SEEDING NEEDLE CARTRIDGE SYSTEM, INDIGO LASEROPTIC TREATMENT SYSTEM, INDIGO PORTABLE LASER SYSTEM WITH TEMPERATURE FEEDBACK -MODEL IDL 830 (POWER OPTIONS : 25, 20, 15 & 10 WATTS) INDIGO FIB

View 6 510(k) Devices ↓

6

Total

6

Cleared

0

Denied

Indigo Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Palo Alto, US.

Historical record: 6 cleared submissions from 1996 to 1999. Primary specialty: General & Plastic Surgery.

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

Indigo Medical, Inc. is one of 21528 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

6 devices

1-6 of 6

Cleared Oct 04, 1999

INDIGO PROSTATE SEEDING NEEDLE CARTRIDGE SYSTEM

Radiology · 90d

Cleared Mar 30, 1999

INDIGO LASEROPTIC TREATMENT SYSTEM

General & Plastic Surgery · 15d

Cleared Dec 23, 1997

INDIGO PORTABLE LASER SYSTEM WITH TEMPERATURE FEEDBACK -MODEL IDL 830 (POWER...

General & Plastic Surgery · 446d

Cleared Feb 21, 1997

INDIGO MEDICAL MODEL IDL 830 & MODEL IDL 830E LASER SYSTEMS FOR GENERAL...

General & Plastic Surgery · 197d

Cleared Feb 16, 1996

INDIGO MEDICAL MODEL IDL 830E

General & Plastic Surgery · 59d

Cleared Jan 25, 1996

INDIGO PORTABLE LASER SYSTEM, INDDIGO FIBEROPTICS

General & Plastic Surgery · 141d