FDA 510(k) Application Details - K924019

Device Classification Name Table, Powered

  More FDA Info for this Device
510(K) Number K924019
Device Name Table, Powered
Applicant MIDLAND MFG. CO.
55 NORTHERN BOULEVARD,
SUITE 301
GREAT NECK, NY US
Other 510(k) Applications for this Company
Contact ALAN P SCHWARTZ
Other 510(k) Applications for this Contact
Regulation Number 890.3760

  More FDA Info for this Regulation Number
Classification Product Code INQ
Other 510(k) Applications for this Device

  More FDA Info for this Product Code
Date Received 08/11/1992
Decision Date 11/06/1992
Decision SE - Substantially Equivalent
Classification Advisory Committee NE - Neurology
Review Advisory Committee PM - Physical Medicine
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact