Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K001162
Device Classification Name
Lancet, Blood
More FDA Info for this Device
510(K) Number
K001162
Device Name
Lancet, Blood
Applicant
MALI-TECH LTD.
POB 454
GINOT SHOMRON 44853 IL
Other 510(k) Applications for this Company
Contact
AHAVA STEIN
Other 510(k) Applications for this Contact
Regulation Number
878.4800
More FDA Info for this Regulation Number
Classification Product Code
FMK
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/10/2000
Decision Date
08/09/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
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