Medical Device Manufacturer · US , Stamford , CT

Meditech International, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2003

Recent clearances: BIOFLEX LD-R100 TREATMENT HEAD, LD-I 75 AND LD-I 200, BIOFLEX PRESCRIPTION SYSTEM AND RELATED TREATMENT HEADS

View 5 510(k) Devices ↓

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Meditech International, Inc. Physical Medicine ✕

5 devices

1-5 of 5

Cleared Dec 18, 2008

BIOFLEX LD-R100 TREATMENT HEAD

Physical Medicine · 218d

Cleared Apr 02, 2008

LD-I 75 AND LD-I 200

Physical Medicine · 205d

Cleared Mar 13, 2006

BIOFLEX PRESCRIPTION SYSTEM AND RELATED TREATMENT HEADS

Physical Medicine · 245d

Cleared Feb 24, 2005

BIOFLEX LD-175 AND LD-1200 TREATMENT HEADS

Physical Medicine · 227d

Cleared Apr 10, 2003

BIOFLEX PROFESSIONAL THERAPY SYSTEM

Physical Medicine · 163d