Product code JRQ— Clinical Chemistry

FDA has cleared 8 devices under product code JRQ between 1977 and 1981, filed by 7 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.

• 19813 clearances
• 19801 clearance
• 19792 clearances
• 19781 clearance
• 19771 clearance

• American Dade2 clearances
• Techhnilab Instruments, Inc.1 clearance
• Sysmex Corp.1 clearance
• Scientific Manufacturing Industries1 clearance
• Maddak, Inc.1 clearance
• Dynatech Corp.1 clearance
• American Hospital Supply Corp.1 clearance

• K813318 — MINI-SHAKERDynatech Corp.·1981-12-17
• K813148 — S/P VORTEX MIXERAmerican Dade·1981-11-24
• K813149 — S/P VORTEX MIXER JR.American Dade·1981-11-24
• K801145 — SMI MULTI-TUBE VORTEXERScientific Manufacturing Industries·1980-06-09
• K790753 — DIMENSIONALL ROTATORAmerican Hospital Supply Corp.·1979-06-28
• K790027 — SHAKER, MODEL SH-510Sysmex Corp.·1979-02-08
• K780543 — THERMAJUST CIRCU-TEMPTechhnilab Instruments, Inc.·1978-05-26
• K770165 — MICRO-MIX PIPETTE SHAKERMaddak, Inc.·1977-01-31