510(k) K934724

AESCULAP TROCAR INSTRUMENT SET by Aesculap, Inc. — Product Code FBQ

K934724 is an FDA 510(k) premarket notification submitted by Aesculap, Inc. for the device "AESCULAP TROCAR INSTRUMENT SET". The FDA issued a decision of Substantially Equivalent on December 23, 1993. The device falls under product code FBQ (Trocar, Gastro-Urology), a Class II device regulated under 21 CFR 876.5090. Aesculap, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 23, 1993
Date Received
October 1, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Trocar, Gastro-Urology
Device Class
Class II
Regulation Number
876.5090
Review Panel
SU
Submission Type