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Progress Mankind Technology

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K883314PMT 3721-1 EPIDURAL KITOctober 28, 1988
K881616PMT MANKIND LUMBAR-PERITONEAL SHUNT MODEL 1115-1September 9, 1988
K871663PMT TRACTION TONGSJune 19, 1987
K854157PMT ACCUPRESSURE INFUSION SYSTEM 3601February 13, 1986
K845035ELECTRODE FOR NEUROLOGICAL SURGERY 2111July 30, 1985
K845036TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600June 26, 1985
K834047PMT-HALO/ORTHOPEDIC JACKET SYSTEMFebruary 17, 1984
K831329PMT VAXIOM STEREOTACTIC SYS #FX001June 15, 1983
K830530TEMP TRACEApril 6, 1983
K812744LEVY BIOTAC #LX001 BIOPSY PROBE HOLDERDecember 3, 1981
K810627MODEL 1301 BIOTAC (TM)April 2, 1981
K802151PMT DEPTHALON DEPTH CORTICOGRAPHY ELECNovember 19, 1980
K802152PMT DEPTHALON DEPTH #2102November 19, 1980
K802249MICROLET FAMILY OF NEEDLE/DEPTH ELECT-November 19, 1980
K802243VAXIOM FAMILY OF RF LESION PROBES & ELECNovember 12, 1980
K801134MICROVACMay 30, 1980
K801127MACROVACMay 30, 1980