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

THE AMO OPHTHALMIC SURGICAL SYSTEM

K Number: K060366 · Decision Apr 7, 2006
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
315
Applicant Total
8
Review Days
53

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
THE AMO OPHTHALMIC SURGICAL SYSTEM
K Number
K060366
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
886.4670
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Advanced Medical Optics, Inc.
Date Received
February 13, 2006
Decision Date
April 7, 2006
Product Code
HQC
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
HQC Unit, Phacofragmentation

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HQC), ordered by most recent decision date.

View all

Other Clearances by Advanced Medical Optics, Inc.

K Number Device Name
K081681 VITRECTOMY CUTTER AND ACCESSORIES
K081545 ONE SERIES ULTRA CARTRIDGE, MODEL 1VIPR30
K042562 LENS PLUS REWETTING DROPS
K050648 SOVEREIGN HIGH VACUUM PACK, SOVEREIGN COMPACT HIGH VACUUM PACK
K040839 COMPLETE BLINK-N-CLEAN LENS DROPS
K032030 BLINK CL LUBRICANT EYE DROPS
K030092 COMPLETE BRAND MULTI-PURPOSE SOLUTION