KET — Filters, Cell Collection, Tissue Processing Class I

FDA Device Classification

FDA product code KET covers "Filters, Cell Collection, Tissue Processing", a Class I medical device regulated under 21 CFR 864.3010. Submissions are reviewed by the Pathology panel. At least 5 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
KET
Device Class
Class I
Regulation Number
864.3010
Submission Type
Review Panel
PA
Medical Specialty
Pathology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K875122corning medical and scientificDISPOSABLE STERILE SYRINGE FILTERSJanuary 12, 1988
K870196poreticsPCTE MICROPOROUS MEMBRANE FILTERMay 12, 1987
K844671corning medical and scientificCORNING DISPOSAL STERILE FILTER SYSTEM-NYLONFebruary 25, 1985
K840556corning medical and scientificDISPOSABLE SYRINGE FILTERSMarch 5, 1984
K792633procter and gamble mfgSTERILIZATION PROCESS/OUTERWRAPJanuary 11, 1980