GDI — Dissector, Surgical, General & Plastic Surgery Class I

FDA Device Classification

FDA product code GDI covers "Dissector, Surgical, General & Plastic Surgery", a Class I medical device regulated under 21 CFR 878.4800. Submissions are reviewed by the General, Plastic Surgery panel. At least 7 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
GDI
Device Class
Class I
Regulation Number
878.4800
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K896383galenica enterprisesDISPOSABLE EXTERNAL CLAMPSDecember 6, 1989
K850288beecher medical diagnostic instrumentationHEPATIC PARENCHYMAL SUCTION DISSECTORMarch 18, 1985
K831912ormed mfgROUND-BEEHIVE- DISSECTORS 3/8October 31, 1983
K822569kelleherTYMPANOPLASTY & SKIN DISSECTORSOctober 6, 1982
K803292v. mueller o.v. baxter healthcareFIELD SUCTION DISSECTORJanuary 29, 1981
K791870carwildDISPOSABLE SPECIALITY SPONGESNovember 5, 1979
K791703edward weckTEW BYPASS INSTRUMENTS & DISSECTING KITOctober 4, 1979