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

TM MICRO-CATHETERS

K Number: K971124 · Decision May 16, 1997
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
115
Applicant Total
82
Review Days
50

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Basic Information

Device Name
TM MICRO-CATHETERS
K Number
K971124
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, Inc.
Date Received
March 27, 1997
Decision Date
May 16, 1997
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

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Other Clearances by Xomed, Inc.

K Number Device Name
K002395 MODEL 30 CLASSIC PNEUMATONOMETER
K002987 REDTRONIC XOMED MONOPOLAR ENERGIZED BLADE
K002828 XPS NITRO SYSTEM
K002897 TITANIUM MIDDLE EAR PROSTHESES
K993653 MICRO-FRANCE TROCARS AND ACCESSORIES
K001148 MEROGEL OTOLOGIC PACK
K994262 FRONTAL SINUS TREPHINATION CANNULA
K992855 XPS STRAIGHTSHOT OR MODEL 2000 MICRODEBRIDER SYSTEM OR XPS POWERSCULPT
K993582 MODIFICATION TO LASER-SHIELD II
K993655 MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS
Search all 82 clearances from Xomed, Inc. →