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

ALCON CONTACT LENS CASE

K Number: K971618 · Decision Jul 14, 1997
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
81
Applicant Total
47
Review Days
73

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Basic Information

Device Name
ALCON CONTACT LENS CASE
K Number
K971618
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5928
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alcon Laboratories
Date Received
May 2, 1997
Decision Date
July 14, 1997
Product Code
LRX
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
LRX Case, Contact Lens

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K990480 OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVER
K984575 MULTI-PURPOSE DISINFECTING SOLUTION ID 90746
K983973 OPTI-ONE MULTI-PURPOSE SOLUTION
K983780 MULTI-PURPOSE DISINFECTING SOLUTION ID 90746
K981561 LIQUID ENZYME ID 90133
K981571 MONARCH IOL DELIVERY SYSTEM
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