Medical Device Manufacturer · US , Lafayette , CA

Tti Medical - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1987

Total

Cleared

Denied

Tti Medical has 9 FDA 510(k) cleared medical devices. Based in Lafayette, US.

Historical record: 9 cleared submissions from 1987 to 1995. Primary specialty: General & Plastic Surgery.

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

Tti Medical 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 - Tti Medical

9 devices

1-9 of 9

Cleared May 31, 1995

ACCU-BEAM FIBER OPTIC HANDPIECE

K952006 · GEX

General & Plastic Surgery · 33d

Cleared May 24, 1995

ACCU-BEAM 300W XENON LIGHT SOURCE

K951895 · GCT

Gastroenterology & Urology · 30d

Cleared Feb 24, 1995

ACCU-BEAM C02 LASER HANDPIECE

K945648 · GEX

General & Plastic Surgery · 99d

Cleared Jun 01, 1993

ACCU-BEAM TUBE SET

K921208 · GCJ

General & Plastic Surgery · 446d

Cleared Nov 07, 1991

ACCU-BEAM LAPAROSCOPIC SYSTEM

K910978 · GEI

General & Plastic Surgery · 245d

Cleared Feb 22, 1990

ACCU-BEAM WAVEGUIDE

K895656 · GEX

General & Plastic Surgery · 156d

Cleared May 15, 1989

ACCU-BEAM YAG FIBER

K890922 · GEX

General & Plastic Surgery · 80d

Cleared Mar 09, 1987

CO2 LASER BRONCHOSCOPE SET

K870063 · EOQ

Ear, Nose, Throat · 61d

Cleared Mar 05, 1987

DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET

K870046 · HHR

Obstetrics & Gynecology · 59d

Tti Medical - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Tti Medical

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