FDA 510(k) Application Details - K972317

Device Classification Name	System, Vocal Cord Medialization   More FDA Info for this Device
510(K) Number	K972317
Device Name	System, Vocal Cord Medialization
Applicant	BOSTON MEDICAL PRODUCTS, INC. 49 PLAIN ST. NORTH ATTLEBORO, MA 02760 US Other 510(k) Applications for this Company
Contact	ROSINA ROBINSON Other 510(k) Applications for this Contact
Regulation Number	874.3620   More FDA Info for this Regulation Number
Classification Product Code	MIX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/20/1997
Decision Date	09/18/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review