Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K980673
Device Classification Name
Bandage, Liquid
More FDA Info for this Device
510(K) Number
K980673
Device Name
Bandage, Liquid
Applicant
INNOVATIVE TECHNOLOGIES (US), INC.
581 CONFERENCE PLACE
GOLDEN,, CO 80401 US
Other 510(k) Applications for this Company
Contact
JULIE CHAFFEE
Other 510(k) Applications for this Contact
Regulation Number
880.5090
More FDA Info for this Regulation Number
Classification Product Code
KMF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/20/1998
Decision Date
05/21/1998
Decision
SN - Substantially Equivalent for Some Indications
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact