Product code JRC— Clinical Chemistry

FDA has cleared 6 devices under product code JRC between 1976 and 1984, filed by 6 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.

• 19842 clearances
• 19821 clearance
• 19801 clearance
• 19771 clearance
• 19761 clearance

• Vitex1 clearance
• Sherwood Medical Industries1 clearance
• Scientific Manufacturing Industries1 clearance
• Meridian Diagnostics, Inc.1 clearance
• American Dade1 clearance
• Abco Dealers, Inc.1 clearance

• K840186 — SMI DIGITRONScientific Manufacturing Industries·1984-04-05
• K834100 — PRE-CALIBRATED PIPETTESVitex·1984-02-21
• K822078 — DADE DISP. DISPENSING-SPREADING PIPETSAmerican Dade·1982-07-27
• K792696 — MICROPITETTEMeridian Diagnostics, Inc.·1980-02-01
• K770594 — LABORATORY EXPENDABLE PRODUCTSAbco Dealers, Inc.·1977-07-06
• K760621 — LANCER PLASTIC TRANSFER PIPETTESherwood Medical Industries·1976-10-05