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

MICROTEK INTRANASAL SPLINT

K Number: K862496 · Decision Jul 14, 1986
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
14
Applicant Total
24
Review Days
13

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Basic Information

Device Name
MICROTEK INTRANASAL SPLINT
K Number
K862496
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.5800
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Microtek Medical, Inc.
Date Received
July 1, 1986
Decision Date
July 14, 1986
Product Code
EPP
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
EPP Splint, Nasal

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K050322 MICROTEK EQUIPMENT DRAPES
K022903 CHILLBUSTER
K020956 VIVOSONIC DIANOSTIC ULTRASOUND IMAGING COUPLING MEDIA
K011318 VENODYNE DVT ADVANTAGE PLUS
K001802 VENODYNE DVT ADVANTAGE MODEL 610
K950906 LESINSKI SURGICAL EAR DRESSING
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