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LGH — Instrument, Cast Removal, Ac-Powered Class I

FDA Device Classification

Classification Details

Product Code
LGH
Device Class
Class I
Regulation Number
888.5960
Submission Type
Review Panel
OR
Medical Specialty
Orthopedic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K932653carapaceSWISSTEK 2000(TM) CAST REMOVAL SYSTEMJanuary 28, 1994
K901677buckman coCARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTERApril 23, 1990
K893380bremer mfg. and tool coQCR SYSTEM I AND QCR SYSTEM IINovember 16, 1989
K895861johnson and johnson professionalsDELTA-TECH(TM) CAST REMOVAL SYSTEMOctober 19, 1989
K873723martin medicalPLASTER VACUUM, 230V MODEL NO. 4183-161December 10, 1987
K873721martin medicalPLASTER VACUUM, 115V MODEL NO. 4183-160December 7, 1987
K873719martin medicalCAST CUTTER, 115V MODEL NO. 4183-106October 2, 1987
K873720martin medicalCAST CUTTER, 230V MODEL NO. 4183-107October 2, 1987
K820351black and decker(tm)CAST CUTTER/CAST SAW/INSTRUMENTMarch 2, 1982