Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K983792
Device Classification Name
Expander, Skin, Inflatable
More FDA Info for this Device
510(K) Number
K983792
Device Name
Expander, Skin, Inflatable
Applicant
SEARE BIOMEDICAL CORP.
3190 CHULA VISTA CIRCLE
SALT LAKE CITY, UT 84121 US
Other 510(k) Applications for this Company
Contact
WILLIAM JOHN SEARE JR
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LCJ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/27/1998
Decision Date
12/11/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact