Product code KER— Pathology

FDA has cleared 5 devices under product code KER between 1977 and 1983, filed by 3 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.

• 19834 clearances
• 19771 clearance

• Surgipath Medical Industries, Inc.2 clearances
• Polymer Technology Corp.2 clearances
• Sherwood Medical Industries1 clearance

• K831922 — EMBEDDING RINGPolymer Technology Corp.·1983-07-29
• K831900 — MACLEAN-FOGG, DISP. BASE MOLDPolymer Technology Corp.·1983-07-28
• K831333 — EMBEDDING RINGSSurgipath Medical Industries, Inc.·1983-05-25
• K831335 — DISPOSABLE BASE MOLDSurgipath Medical Industries, Inc.·1983-05-16
• K772149 — LANCER BIOPSY HOLDERSherwood Medical Industries·1977-11-22