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

ALCON FLUID INJECTOR

K Number: K882723 · Decision Nov 8, 1988
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
2
Applicant Total
47
Review Days
130

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Basic Information

Device Name
ALCON FLUID INJECTOR
K Number
K882723
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1670
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Alcon Laboratories
Date Received
July 1, 1988
Decision Date
November 8, 1988
Product Code
DQF
Advisory Committee
Cardiovascular
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
DQF Actuator, Syringe, Injector Type

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Other Clearances by Alcon Laboratories

K Number Device Name
K062624 NEXT GENERATION LASER
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K000148 RGP MULTI-PURPOSE SOLUTION ID 100136
K984573 OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP
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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