Atlas FDA

Preset Tips

FDA premarket approval P080004/S017 · decided 2018-08-06

Approval details

PMA number
P080004
Supplement
S017
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Preset Tips
Generic name
intraocular lens
Applicant
Hoya Surgical Optics, Inc.
Date received
2017-04-10
Decision date
2018-08-06
Days to decision
483 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Chino Hills, CA
Statement
Approval for modifications to the injector tip acceptance criteria.

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510(k) clearances by this applicant

RecordFirmDate
HOYA IS INJECTOR SYSTEM (K081346)Hoya Surgical Optics, Inc.2009-03-23