Product code GRE— Microbiology

FDA has cleared 4 devices under product code GRE between 1977 and 1988, 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.

• 19881 clearance
• 19851 clearance
• 19821 clearance
• 19771 clearance

• Microbiological Assoc.1 clearance
• Idt, A Division of Whittaker M.A. Bioproducts1 clearance
• Gull Laboratories, Inc.1 clearance
• Electro-Nucleonics Laboratories, Inc.1 clearance

• K884004 — RUBEOLA TESTGull Laboratories, Inc.·1988-12-05
• K853067 — FIAX TEST KIT FOR MEASLES-G ANTIBODIES FLYORESCENTIdt, A Division of Whittaker M.A. Bioproducts·1985-10-22
• K821249 — ENI ANTIBODY TO MEASLES(RUBEOLA) VIRUSElectro-Nucleonics Laboratories, Inc.·1982-07-30
• K770687 — MEASLESVIRUS FLOURE. CONJUGATED ANTISERUMicrobiological Assoc.·1977-06-14