Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K223480
Device Classification Name
More FDA Info for this Device
510(K) Number
K223480
Device Name
Medipoint Blood Lancets
Applicant
Medipoint Holdings, LLC
72 East 2nd St.
Mineola, NY 11501 US
Other 510(k) Applications for this Company
Contact
Rochelle Stern
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
QRK
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/18/2022
Decision Date
01/13/2023
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