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Medical Products Development, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K810012MULTIMICRO SURGICAL CAUTERYApril 23, 1981
K810016REPLACABLE BATTERY PERFECTEMP CAUTERYApril 23, 1981
K810013MULTIPERFECTEMP CAUTERYApril 23, 1981
K803067SURG-FLEX 10 LIGHTFebruary 26, 1981
K810015MULTIHI-TEMP CAUTERYFebruary 12, 1981
K810014REPLACABLE BATTERY HI-TEMP CAUTERYFebruary 12, 1981
K802942HITEMP. TM 2 LOOPTIP CAUTERYFebruary 4, 1981
K810019SURG-FLEX 15 SURGICAL LIGHTJanuary 23, 1981
K810018SURG-FLEX 5 SURGICAL LIGHTJanuary 23, 1981
K810017MICROSURG CAUTERYJanuary 5, 1981
K802330HI-TEMP LOOPTIP SURGICAL CAUTERYNovember 12, 1980
K801323HI-TEMP SURGICAL CAUTERYJune 26, 1980
K801078PERFECTEMP OPHTHALMIC CAUTERYJune 4, 1980