FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

TYMPANOSTOMY (VENTILATION) TUBE

K Number: K941407 · Decision Mar 14, 1995
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
115
Applicant Total
12
Review Days
356

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Basic Information

Device Name
TYMPANOSTOMY (VENTILATION) TUBE
K Number
K941407
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3880
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Xomed-Treace, Inc.
Date Received
March 23, 1994
Decision Date
March 14, 1995
Product Code
ETD
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ETD Tube, Tympanostomy

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ETD), ordered by most recent decision date.

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Other Clearances by Xomed-Treace, Inc.

K Number Device Name
K940028 ENDOSCOPE SHEATH
K945659 BLACKSTAR(TM) STAR SYSTEM
K932771 BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCE
K933672 XOMED-TREACE SCOPESHEATH
K934426 NERVE INTEGRITY MONITOR-2 (NIM-2 XL)
K933105 XOMED-TREACE RIGID ROD LENS ENDOSCOPE
K925640 XOMED-TREACE EMG ENDOTRACHEAL TUBEEN
K922880 XOMED TREACE JET VENTILATION TUBE
K923830 XOMED-TREACE ALPHASCOPE
K912753 XOMED-TREACE POSITROL FOOTPEDAL SUCTION CONTROL
Search all 12 clearances from Xomed-Treace, Inc. →