Product code GJG— Hematology

FDA has cleared 4 devices under product code GJG between 1976 and 1983, 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.

• 19831 clearance
• 19782 clearances
• 19761 clearance

• The Kendall Company Div. of Tyco Healthcare Group1 clearance
• Owens-Illinois, Inc.1 clearance
• Hillwood Corp.1 clearance
• Dade, Baxter Travenol Diagnostics, Inc.1 clearance

• K831079 — LIQUIPETTEThe Kendall Company Div. of Tyco Healthcare Group·1983-04-28
• K781891 — PIPETTES, PLASTIC DISPOSABLEHillwood Corp.·1978-11-15
• K780237 — DISPOSABLE CONTROLLED DROP PASTEUR PIPETOwens-Illinois, Inc.·1978-03-09
• K760719 — UNIFORM DROP SIZE PASTEUR TYPE PIPETSDade, Baxter Travenol Diagnostics, Inc.·1976-10-29