Product code MJG— General, Plastic Surgery

FDA has cleared 7 devices under product code MJG between 1993 and 2008, 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.

• 20081 clearance
• 20071 clearance
• 19991 clearance
• 19961 clearance
• 19941 clearance
• 19932 clearances

• Sts Biopolymers1 clearance
• PAJUNK GmbH Medizintechnologie1 clearance
• Nhr, Inc.1 clearance
• Contour Fabricators of Florida, Inc.1 clearance
• Clevex, Inc.1 clearance
• Buckman Co., Inc.1 clearance
• Bip USA, Inc.1 clearance

• K080674 — PAJUNK'S PRIMOCUT DISPOSABLE BIOPSY SYSTEMPAJUNK GmbH Medizintechnologie·2008-05-09
• K070836 — EXICLIP EXCS-MClevex, Inc.·2007-04-20
• K983647 — ECHO-COAT ULTRASOUND NEEDLESSts Biopolymers·1999-01-20
• K955683 — RNS STERILE, DISPOSABLE BREAST BIOPSY/LOCALIZATION TRAYContour Fabricators of Florida, Inc.·1996-02-01
• K933324 — SKIN BIOPSY DEVICENhr, Inc.·1994-03-31
• K925870 — SPACERBip USA, Inc.·1993-05-19
• K922919 — DYNACYT BIOPSY ASPIRATION DEVICEBuckman Co., Inc.·1993-03-31