Product code DMP— Clinical Toxicology

FDA has cleared 4 devices under product code DMP between 1977 and 1997, 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.

• 19971 clearance
• 19951 clearance
• 19781 clearance
• 19771 clearance

• Pcl-Ria, Inc.1 clearance
• Nuclear Medical Laboratories, Inc.1 clearance
• Chimera Research & Chemical, Inc.1 clearance
• Boehringer Mannheim Corp.1 clearance

• K973973 — ELECSYS CALLCHECK DIGOXINBoehringer Mannheim Corp.·1997-11-04
• K953393 — TOX PERFECT A TUBEChimera Research & Chemical, Inc.·1995-10-06
• K780889 — DIGOXIN STANDARDS IN HUMAN SERUMPcl-Ria, Inc.·1978-08-14
• K770411 — DIGI TROL TM-RX & DIGI TROL TM-TXNuclear Medical Laboratories, Inc.·1977-03-16