Atlas FDA

MENICON SF-P (TM)

FDA premarket approval P880098/S011 · decided 2000-09-06

Approval details

PMA number
P880098
Supplement
S011
Supplement type
Normal 180 Day Track
Supplement reason
Postapproval Study Protocol
Trade name
MENICON SF-P (TM)
Generic name
Lens, contact (other material) - daily
Applicant
Menicon Co, Ltd.
Date received
2000-06-13
Decision date
2000-09-06
Days to decision
85 days
Decision code
APPR
Product code
HQD
Advisory committee
Ophthalmic
Expedited review
No
Location
Wilmington, MA
Statement
APPROVAL OF PROCEDURES TO ADD LENS FINISHING LABORATORIES AS MANUFACTURERS AND DISTRIBUTORS OF CLASS III RGP EXTENDED WEAR CONTACT LENSES.

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510(k) clearances by this applicant

RecordFirmDate
Miru 1day UpSide (midafilcon A) (K193399)Menicon Co, Ltd.2020-06-17
Menicon 3% Hydrogen Peroxide Cleaning and Disinfecting Solution (K191872)Menicon Co, Ltd.2020-03-02
One Day Flat Pack (hioxifilcon A) Daily Disposable Soft Contact Lens (K180819)Menicon Co, Ltd.2018-05-16
Menicon ASRB (asmofilcon A) Silicone Hydrogel Soft Contact Lens (K180004)Menicon Co, Ltd.2018-02-22
Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses (K173136)Menicon Co, Ltd.2017-11-16
Menicon Saline Rinse Solution (K151768)Menicon Co, Ltd.2015-08-28
MENICON UNIQUE PH MULTI-PURPOSE SOLUTION (K130805)Menicon Co, Ltd.2013-07-03
MENICON PROGENT PROTEIN REMOVER FOR RIGID GAS PERMEABLE CONTACT LENS (K122273)Menicon Co, Ltd.2013-01-02