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

ALCON SURGICAL PROCEDURE PACKS

K Number: K880961 · Decision Apr 29, 1988
Classifications
1
FEI Numbers
165
Registration Numbers
165
Same Product Code
109
Applicant Total
47
Review Days
52

Basic Information

Device Name
ALCON SURGICAL PROCEDURE PACKS
K Number
K880961
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
ALCON LABORATORIES
Date Received
March 8, 1988
Decision Date
April 29, 1988
Product Code
LRO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
LRO General Surgery Tray

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K Number Device Name
K062624 NEXT GENERATION LASER
K062865 SMALL VOLUME SYRINGE
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
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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