FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

POPE OTO-WICK, STERILE & NON-STERILE

K Number: K791059 · Decision Jul 17, 1979
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
3
Applicant Total
82
Review Days
39

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Basic Information

Device Name
POPE OTO-WICK, STERILE & NON-STERILE
K Number
K791059
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.5220
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Xomed, Inc.
Date Received
June 8, 1979
Decision Date
July 17, 1979
Product Code
KCN
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
KCN Ear Wick

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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. →