Product code GCD— General, Plastic Surgery

FDA has cleared 8 devices under product code GCD between 1976 and 1995, 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.

• 19951 clearance
• 19941 clearance
• 19861 clearance
• 19852 clearances
• 19763 clearances

• Sil-Med Corp.2 clearances
• Sherwood Medical Industries1 clearance
• R-Group Intl.1 clearance
• Luther Medical Products, Inc.1 clearance
• Ipco Corp.1 clearance
• B. Braun Instruments1 clearance
• Angiomed U.S., Inc.1 clearance

• K952470 — ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II.R-Group Intl.·1995-11-28
• K940198 — L-CATH CONNECTOR ASSEMBLYLuther Medical Products, Inc.·1994-12-15
• K863446 — ANGIOMED HIGH PRESSURE CONNECTORSAngiomed U.S., Inc.·1986-09-23
• K851196 — INCISION DRAINSil-Med Corp.·1985-06-04
• K851921 — Y CONNECTORSil-Med Corp.·1985-05-17
• K760382 — CONNECTORSB. Braun Instruments·1976-11-02
• K760524 — CATHETER CONNECTOR, ARGYLE TUBINGSherwood Medical Industries·1976-11-02
• K760203 — TUBE, STERILE NON-CONDUCTIVE CONNECTINGIpco Corp.·1976-07-19