Medical Device Manufacturer · US , Worcester , MA

Cambridge Biotech Corp. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1991

Recent clearances: CAMBRIDGE BIOTECH HUMAN LYME IGG WESTERN BLOT (90111), CAMBRIDGE BIOTECH HUMAN LYME IGM WESTERN BLOT (90112), CYTOCLONE A & B EIA

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cambridge Biotech Corp. Microbiology ✕

3 devices

1-3 of 3

Cleared Feb 17, 1998

CAMBRIDGE BIOTECH HUMAN LYME IGG WESTERN BLOT (90111)

Microbiology · 326d

Cleared Feb 17, 1998

CAMBRIDGE BIOTECH HUMAN LYME IGM WESTERN BLOT (90112)

Microbiology · 326d

Cleared Jul 30, 1991

CYTOCLONE A & B EIA

Microbiology · 88d