Product code IDZ— Pathology

FDA has cleared 5 devices under product code IDZ between 1976 and 1986, filed by 4 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19862 clearances
• 19832 clearances
• 19761 clearance

• Surgipath Medical Industries, Inc.2 clearances
• Sherwood Medical Industries1 clearance
• Polymer Technology Corp.1 clearance
• Australian Biomedical Corporation , Ltd.1 clearance

• K863483 — CASSETTE EMBOSSEERSurgipath Medical Industries, Inc.·1986-09-16
• K862457 — LYNX EL MICROSCOPY TISSUE PROCESSORAustralian Biomedical Corporation , Ltd.·1986-07-16
• K833857 — MACLEAN-FOGG, TISSUE CASSETTESPolymer Technology Corp.·1983-12-02
• K831334 — TISSUE CASSETTES FOR PROCESSING-EM BEDSurgipath Medical Industries, Inc.·1983-05-25
• K760623 — LANCER PARAPLAST HISTO PROCESS CASSETTESherwood Medical Industries·1976-09-27