510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Progress Mankind Technology

Hopkins, MN, US

Progress Mankind Technology appears in FDA device records in Hopkins, MN. FDA records list 17 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
17
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 17 510(k) clearances for Progress Mankind Technology between 1980 and 1988. The busiest year on record is 1980, with 6. The most recent is 1988, with 2.

Clearances by year, as a table
510(k) clearance decisions for Progress Mankind Technology, by decision year
YearClearances
19806
19812
19832
19841
19852
19861
19871
19882
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K883314PMT 3721-1 EPIDURAL KITCAZSubstantially Equivalent
K881616PMT MANKIND LUMBAR-PERITONEAL SHUNT MODEL 1115-1JXGSubstantially Equivalent
K871663PMT TRACTION TONGSHAXSubstantially Equivalent
K854157PMT ACCUPRESSURE INFUSION SYSTEM 3601FRNSubstantially Equivalent
K845035ELECTRODE FOR NEUROLOGICAL SURGERY 2111GYCSubstantially Equivalent for Some Indications
K845036TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600LCJSubstantially Equivalent
K834047PMT-HALO/ORTHOPEDIC JACKET SYSTEMHAXSubstantially Equivalent
K831329PMT VAXIOM STEREOTACTIC SYS #FX001HAWSubstantially Equivalent
K830530TEMP TRACEFLLSubstantially Equivalent
K812744LEVY BIOTAC #LX001 BIOPSY PROBE HOLDERHAWSubstantially Equivalent
K810627MODEL 1301 BIOTAC (TM)GEASubstantially Equivalent
K802249MICROLET FAMILY OF NEEDLE/DEPTH ELECT-GZLSubstantially Equivalent
K802152PMT DEPTHALON DEPTH #2102GZLSubstantially Equivalent
K802151PMT DEPTHALON DEPTH CORTICOGRAPHY ELECGZLSubstantially Equivalent
K802243VAXIOM FAMILY OF RF LESION PROBES & ELECGXISubstantially Equivalent
K801134MICROVACJOLSubstantially Equivalent
K801127MACROVACJOLSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain