Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by INSIGHT TECHNOLOGIES INSTRUMENTS, LLC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K974243
11/12/1997
KERATOME SYSTEM
INSIGHT TECHNOLOGIES INSTRUMENTS, LLC.
K984537
12/21/1998
KERATOME SYSTEM, MODEL K3000
INSIGHT TECHNOLOGIES INSTRUMENTS, LLC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact