Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by WINDY HILL TECHNOLOGY, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K993342
10/05/1999
DUCPREP BREAST ASPIRATOR, MODEL PMPO2
WINDY HILL TECHNOLOGY, INC.
K983867
11/02/1998
FUJI CATHETER, MODEL CTH001
WINDY HILL TECHNOLOGY, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact