510(k) K062672

GRACE MEDICAL PC COATED TYMPANOSTOMY TUBES by Grace Medical, Inc. — Product Code ETD

K062672 is an FDA 510(k) premarket notification submitted by Grace Medical, Inc. for the device "GRACE MEDICAL PC COATED TYMPANOSTOMY TUBES". The FDA issued a decision of Substantially Equivalent on October 24, 2006. The device falls under product code ETD (Tube, Tympanostomy), a Class II device regulated under 21 CFR 874.3880. Grace Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 24, 2006
Date Received
September 8, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tube, Tympanostomy
Device Class
Class II
Regulation Number
874.3880
Review Panel
EN
Submission Type