Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by TIMOTHY WILLIAMS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K001044
03/31/2000
ACME SPINE SYSTEM - SERIES 6000, 7000, MONOAXIAL AND POLYAXIAL SCREW SYSTEM
ACME SPINE, LLC.
K010649
03/05/2001
EXHALE DOPPLER SYSTEM
BRONCUS TECHNOLOGIES, INC.
K013111
09/18/2001
EXHALE PROBE
BRONCUS TECHNOLOGIES, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact