FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CAST CUTTER, 230V MODEL NO. 4183-107

K Number: K873720 · Decision Oct 2, 1987
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
8
Applicant Total
14
Review Days
17

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Basic Information

Device Name
CAST CUTTER, 230V MODEL NO. 4183-107
K Number
K873720
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.5960
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Martin Medical
Date Received
September 15, 1987
Decision Date
October 2, 1987
Product Code
LGH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LGH Instrument, Cast Removal, Ac-Powered

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Other Clearances by Martin Medical

K Number Device Name
K873723 PLASTER VACUUM, 230V MODEL NO. 4183-161
K873721 PLASTER VACUUM, 115V MODEL NO. 4183-160
K873719 CAST CUTTER, 115V MODEL NO. 4183-106
K873717 CUSHION TREAD WALKING HEEL PRODUCT NO. 4183-135
K873716 ADULT WALKING HEEL PRODUCT NO. 4183-130
K873722 PEDESTAL WALKING HEEL PRODUCT NO. 4183-133
K873718 CHILD WALKING HEEL PRODUCT NO. 4183-132
K863273 MARTIN MEDICAL PRO-SCOPE ANOSCOPE
K863275 MARTIN MEDICAL PRO-SPEC SMALL VAGINAL SPECULUM
K863274 MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM
Search all 14 clearances from Martin Medical →