Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by VISIJET, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K991124
04/02/1999
VISIJET HYDROKERATOME, MODEL 50
VISIJET, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact