Product code GRZ— Microbiology

FDA has cleared 5 devices under product code GRZ between 1984 and 1996, 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.

• 19961 clearance
• 19951 clearance
• 19941 clearance
• 19861 clearance
• 19841 clearance

• Zeus Scientific, Inc.2 clearances
• Zeus Technologies1 clearance
• Whittaker Bioproducts, Inc.1 clearance
• Fuller Laboratories, Inc.1 clearance

• K946373 — MYCOPLASMA SLURRY AND MYCOPLASMA CROWNTITRE IFA TEST SYSTEMZeus Scientific, Inc.·1996-02-07
• K944417 — ZEUA MYCOPLASMAZeus Scientific, Inc.·1995-08-01
• K931557 — FULLER LABORATORIES MYCOPLASM PNEUMONIA IFA-IGG TESTFuller Laboratories, Inc.·1994-03-11
• K861716 — FIAX TEST KIT FOR MYCOPLASMA PNEUMONIAE-G ANTIBODYWhittaker Bioproducts, Inc.·1986-08-08
• K840012 — INDIRECT FLUORESCENT ANTIBODY MYCOZeus Technologies·1984-02-27