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

ZYOPTIX XP EPI SEPARATOR SYSTEM

K Number: K062465 · Decision Sep 6, 2006
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
82
Applicant Total
92
Review Days
13

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Basic Information

Device Name
ZYOPTIX XP EPI SEPARATOR SYSTEM
K Number
K062465
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4370
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bausch & Lomb, Inc.
Date Received
August 24, 2006
Decision Date
September 6, 2006
Product Code
HNO
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HNO Keratome, Ac-Powered

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