FDA 510(k) Application Details - K896116

Device Classification Name Filter, Bacterial, Breathing-Circuit

  More FDA Info for this Device
510(K) Number K896116
Device Name Filter, Bacterial, Breathing-Circuit
Applicant CADEMA MEDICAL PRODUCTS, INC.
P.O. BOX 250
MIDDLETOWN, NY US
Other 510(k) Applications for this Company
Contact KATHLEEN D BORDONI
Other 510(k) Applications for this Contact
Regulation Number 868.5260

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

  More FDA Info for this Product Code
Date Received 10/20/1989
Decision Date 11/17/1989
Decision SE - Substantially Equivalent
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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