Product code JRM— Clinical Chemistry

FDA has cleared 7 devices under product code JRM between 1979 and 1992, 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.

• 19924 clearances
• 19911 clearance
• 19891 clearance
• 19791 clearance

• Mnlase, Inc.4 clearances
• Taylor Corp.1 clearance
• Sherwood Medical Industries1 clearance
• Saniserv, Inc.1 clearance

• K921568 — ORS-100Mnlase, Inc.·1992-06-09
• K921569 — ORS-200Mnlase, Inc.·1992-06-09
• K921570 — ORS-300Mnlase, Inc.·1992-06-09
• K915427 — ORS-1000Mnlase, Inc.·1992-01-07
• K913777 — SELF-CONTAINED SURGICAL SLUSH FREEZERTaylor Corp.·1991-09-25
• K894006 — SANISERV SURGICAL SLUSH SYSTEMSaniserv, Inc.·1989-11-03
• K782077 — LANCER ICE CUBESherwood Medical Industries·1979-04-03