510(k) K932265

SYMBIOSIS DISPOS PULMON BIOPSY FORCEPS W/REUS HAND by Symbiosis Corp. — Product Code FCL

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 9, 1993
Date Received
April 20, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Forceps, Biopsy, Non-Electric
Device Class
Class I
Regulation Number
876.1075
Review Panel
GU
Submission Type