FDA 510(k) Application Details - K771685

Device Classification Name System, Signal Isolation

  More FDA Info for this Device
510(K) Number K771685
Device Name System, Signal Isolation
Applicant HONEYWELL, INC.

, US
Other 510(k) Applications for this Company
Regulation Number 870.2600

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

  More FDA Info for this Product Code
Date Received 09/06/1977
Decision Date 09/14/1977
Decision SE - Substantially Equivalent
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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