KYD — Strip, Schirmer Class I

FDA Device Classification

Classification Details

Product Code
KYD
Device Class
Class I
Regulation Number
886.1800
Submission Type
Review Panel
OP
Medical Specialty
Ophthalmic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K911734northland cataract and eye care clinicTEARTEC RAPID LACRIMAL ASSESMENT SYSTEMNovember 7, 1991
K881515visionexTEAR VOLUME TESTSMay 23, 1988
K832181smith and nephewSNO STRIPS STERILE TEARFLOW TEST STRIPAugust 12, 1983