FDA 510(k) Application Details - K844734

Device Classification Name System, Dialysate Delivery, Central Multiple Patient

  More FDA Info for this Device
510(K) Number K844734
Device Name System, Dialysate Delivery, Central Multiple Patient
Applicant ALCIDE CORP.
125 MAIN ST.
WESTPORT, CT US
Other 510(k) Applications for this Company
Contact HARRY M KAUFMAN
Other 510(k) Applications for this Contact
Regulation Number 876.5820

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

  More FDA Info for this Product Code
Date Received 12/04/1984
Decision Date 05/17/1985
Decision SE - Substantially Equivalent
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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