Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by MEDISISS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100543
02/25/2010
MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01
MEDISISS
K081559
06/03/2008
GENESIS
MEDISISS
K042659
09/28/2004
MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS
MEDISISS
K113028
10/11/2011
MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURS
MEDISISS
K030598
02/25/2003
MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS
MEDISISS
K030919
03/24/2003
SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES
MEDISISS
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact