Product code GEE— General, Plastic Surgery

FDA has cleared 7 devices under product code GEE between 1979 and 1985, 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.

• 19851 clearance
• 19841 clearance
• 19822 clearances
• 19811 clearance
• 19801 clearance
• 19791 clearance

• Van-Tec, Inc.1 clearance
• Ursus Konsult AB1 clearance
• Premier Dental Products Co.1 clearance
• Medi-Spec1 clearance
• Johannah Medical Services, Inc.1 clearance
• Co-Medical, Inc.1 clearance
• American Endoscopy, Inc.1 clearance

• K854003 — STERILE SOFT TISSUE BIOPSY NEEDLECo-Medical, Inc.·1985-10-18
• K841008 — BIOPSY PUNCH, VARIOUSPremier Dental Products Co.·1984-06-08
• K822490 — DEFLECTING CYTOLOGY BRUSHVan-Tec, Inc.·1982-09-14
• K820259 — STERILE CYTOLOGY BRUSHESAmerican Endoscopy, Inc.·1982-03-05
• K812694 — WHISK-RMedi-Spec·1981-10-26
• K801304 — CAMLOC SYRINGE BIOPSY KITJohannah Medical Services, Inc.·1980-06-17
• K792316 — TROTEX II SCREW NEEDLE BIOPSY INSTR. SETUrsus Konsult AB·1979-12-18