Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K172690
Device Classification Name
Stimulator, Nerve, Peripheral, Electric
More FDA Info for this Device
510(K) Number
K172690
Device Name
Stimulator, Nerve, Peripheral, Electric
Applicant
Idmed
Hotel Technoptic - 2 rue Marc Donadille
Marseille 13013 FR
Other 510(k) Applications for this Company
Contact
FrΘdΘric BERNERT
Other 510(k) Applications for this Contact
Regulation Number
868.2775
More FDA Info for this Regulation Number
Classification Product Code
KOI
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/06/2017
Decision Date
05/31/2018
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact