FDA 510(k) Applications Submitted by CAMBRIDGE BIOTECH CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K971169 03/28/1997 CAMBRIDGE BIOTECH HUMAN LYME IGG WESTERN BLOT (90111) CAMBRIDGE BIOTECH CORP.
K971170 03/28/1997 CAMBRIDGE BIOTECH HUMAN LYME IGM WESTERN BLOT (90112) CAMBRIDGE BIOTECH CORP.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact