Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K972138
Device Classification Name
Wrap, Sterilization
More FDA Info for this Device
510(K) Number
K972138
Device Name
Wrap, Sterilization
Applicant
CARR METAL PRODUCTS, INC.
3735 NORTH ARLINGTON AVE.
INDIANAPOLIS, IN 46218 US
Other 510(k) Applications for this Company
Contact
ALAN BOOKER
Other 510(k) Applications for this Contact
Regulation Number
880.6850
More FDA Info for this Regulation Number
Classification Product Code
FRG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/06/1997
Decision Date
11/13/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact