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

ALCON SITE(R)-COMPATIBLE CASSETTE

K Number: K881682 · Decision Jul 1, 1988
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
39
Applicant Total
47
Review Days
73

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Basic Information

Device Name
ALCON SITE(R)-COMPATIBLE CASSETTE
K Number
K881682
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4360
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Alcon Laboratories
Date Received
April 19, 1988
Decision Date
July 1, 1988
Product Code
KYG
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
KYG Device, Irrigation, Ocular Surgery

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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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