510(k) K943849

GROMMENT STYLE VENTURI TUBE by Micromed Development Corp. — Product Code ETD

K943849 is an FDA 510(k) premarket notification submitted by Micromed Development Corp. for the device "GROMMENT STYLE VENTURI TUBE". The FDA issued a decision of Substantially Equivalent on September 2, 1994. The device falls under product code ETD (Tube, Tympanostomy), a Class II device regulated under 21 CFR 874.3880. Micromed Development Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 2, 1994
Date Received
August 4, 1994
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