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Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Maximum Performance Technologies, Mpts, Inc. — Predicate Candidate Screening

11 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

87 daysmedian FDA review time
386 days90th percentile
11clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K903148CHALLENGE 3000 NEUROLOGICAL BOOSTERMaximum Performance Technologies, Mpts, Inc.1991-12-105100
K904360CHALLENGE 4010 ONE CHANNEL WIDE PULSE STIMULATORMaximum Performance Technologies, Mpts, Inc.1991-10-153860
K903149CHANLLENGE 1010 PATIENT KEY PROGRAM STATIONMaximum Performance Technologies, Mpts, Inc.1990-11-051100
K902514CHALLENGE 5010 POWERED MUSCLE STIMULATORMaximum Performance Technologies, Mpts, Inc.1990-08-31870
K902513CHALLENGE 6010 POWERED MUSCLE STIMULATORMaximum Performance Technologies, Mpts, Inc.1990-08-31870
K902511CHALLENGE 7010 POWERED MUSCLE STIMULATORMaximum Performance Technologies, Mpts, Inc.1990-08-31870
K902512CHALLENGE 8000 POWERED MUSCLE STIMULATORMaximum Performance Technologies, Mpts, Inc.1990-08-31870
K901770CHALLENGE 7000 POWERED MUSCLE STIMULATORMaximum Performance Technologies, Mpts, Inc.1990-07-03760
K901769CHALLENGE 6000 POWERED MUSCLE STIMULATORMaximum Performance Technologies, Mpts, Inc.1990-07-03760
K901768CHALLENGE 5000 POWERED MUSCLE STIMULATORMaximum Performance Technologies, Mpts, Inc.1990-07-03760
K901326CHALLENGE 20 POWERED MUSCLE STIMULATORMaximum Performance Technologies, Mpts, Inc.1990-05-29690

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda