IDZ — Cassettes, Tissue Class I

FDA Device Classification

FDA product code IDZ covers "Cassettes, Tissue", 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
IDZ
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
K863483surgipath medical industriesCASSETTE EMBOSSEERSeptember 16, 1986
K862457australian biomedical corporationLYNX EL MICROSCOPY TISSUE PROCESSORJuly 16, 1986
K833857polymer technologyMACLEAN-FOGG, TISSUE CASSETTESDecember 2, 1983
K831334surgipath medical industriesTISSUE CASSETTES FOR PROCESSING-EM BEDMay 25, 1983
K760623sherwood medical industriesLANCER PARAPLAST HISTO PROCESS CASSETTESeptember 27, 1976