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HLF — Device, Measuring, Lens Radius, Ophthalmic Class I

FDA Device Classification

Classification Details

Product Code
HLF
Device Class
Class I
Regulation Number
886.1430
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K930437marco ophthalmicMARCO STANDARD RADIUSGAUGESAugust 9, 1993
K862517bausch and lombBAUSCH & LOMB CONTACT LENS VIEWERAugust 11, 1986
K823767life-tech intlERG-JET ELECTRODEJanuary 8, 1983