Atlas FDA

VIEWPOINT CK SYSTEM

FDA premarket approval P010018/S006 · decided 2004-01-15

Approval details

PMA number
P010018
Supplement
S006
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
VIEWPOINT CK SYSTEM
Generic name
Electrosurgical, radio frequency, refractive correction
Applicant
Refractec, Inc.
Date received
2003-12-04
Decision date
2004-01-15
Days to decision
42 days
Decision code
APPR
Product code
MWD
Advisory committee
Ophthalmic
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL FOR AN ALTERNATE MANUFACTURING SITE FOR THE SUB-ASSEMBLY OF THE RCS-300 CONSOLE COMPONENT AT STELLARTECH RESEARCH CORP., SUNNYVALE, CALIFORNIA.

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510(k) clearances by this applicant

RecordFirmDate
OPTIPOINT CORNEAL MARKER, MODEL VPT-OPT-450 (K053475)Refractec, Inc.2006-03-03
REFRACTEC MCS-100 (K980522)Refractec, Inc.1998-07-22