Product code GBB— General, Plastic Surgery

FDA has cleared 8 devices under product code GBB between 1982 and 1996, filed by 6 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
• 19891 clearance
• 19832 clearances
• 19824 clearances

• Kelleher Corp.3 clearances
• Tenet Medical Engineering1 clearance
• Storz Instrument Co.1 clearance
• Midmark Corp.1 clearance
• Medlog GmbH Marketing Services1 clearance
• Arthro-Medic, Inc.1 clearance

• K964102 — TENET TIBIAL FRACTURE SUPPORTTenet Medical Engineering·1996-12-05
• K893598 — HYDRAULIC FOOT OPERATED STOOLArthro-Medic, Inc.·1989-10-10
• K831325 — NUTROMATMedlog GmbH Marketing Services·1983-06-02
• K831385 — LITHOTOMY CHAIR #415Midmark Corp.·1983-06-02
• K822264 — NAGASHIMA SN OPERATOR'S CHAIRKelleher Corp.·1982-10-13
• K822251 — EXAMINATION & TREATMENT CHAIRSKelleher Corp.·1982-08-27
• K822013 — NAGASHIMA SN AUTOMATIC TREATMENT CHAIRKelleher Corp.·1982-07-28
• K820636 — STORZ #6500 POWER EXAMINATION CHAIRStorz Instrument Co.·1982-03-26