Product code JTQ— Microbiology

FDA has cleared 12 devices under product code JTQ between 1977 and 1988, filed by 10 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.

• 19881 clearance
• 19851 clearance
• 19834 clearances
• 19821 clearance
• 19812 clearances
• 19801 clearance
• 19791 clearance
• 19771 clearance

• Boekel Industries, Inc.2 clearances
• Bionetic Laboratory Products2 clearances
• Thermolyne Corp.1 clearance
• Sybron Corp.1 clearance
• Sterling Drug, Inc.1 clearance
• Scientific Sales Intl., Inc.1 clearance
• Remel Co.1 clearance
• Mdt Corp., Inc.1 clearance
• Forma Scientific, Inc.1 clearance
• Flow Laboratories, Inc.1 clearance

• K875275 — WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMERSterling Drug, Inc.·1988-01-27
• K853379 — PLATE INCUBATORScientific Sales Intl., Inc.·1985-09-03
• K831592 — ANHYDRIC INCUBATORS, CULTURE INCUBATORBoekel Industries, Inc.·1983-06-16
• K830322 — C.A.T. REAGENT KITRemel Co.·1983-03-28
• K830227 — AUTOMATED ELISA READER LBI 300Bionetic Laboratory Products·1983-03-10
• K830405 — LBI-100 37DEGREES INCUBATORBionetic Laboratory Products·1983-03-10
• K822564 — WATER BATHBoekel Industries, Inc.·1982-09-14
• K812826 — FORMA CH/P GAS PROCESSORForma Scientific, Inc.·1981-10-23
• K812340 — TITERTEK MICROPLATE INCUBATORFlow Laboratories, Inc.·1981-09-23
• K801462 — SPOR-O-THERMMdt Corp., Inc.·1980-07-28
• K792060 — TEMPTRONIC 100 WATER BATHSybron Corp.·1979-12-04
• K760928 — BLOOD BANK DRI-BATHThermolyne Corp.·1977-01-10