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

OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVER/ALCON WETTING, SOAKING, CONDITIONING AND DISINFECTING SOLUTION ID 84392

K Number: K981151 · Decision Jun 22, 1998
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
119
Applicant Total
47
Review Days
84

Basic Information

Device Name
OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVER/ALCON WETTING, SOAKING, CONDITIONING AND DISINFECTING SOLUTION ID 84392
K Number
K981151
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
March 30, 1998
Decision Date
June 22, 1998
Product Code
LPN
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
LPN Accessories, Soft Lens Products

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