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

Advanced Medical Products, Inc. — Predicate Candidate Screening

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

87 daysmedian FDA review time
241 days90th percentile
14clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K000932ARACHNOPHLEBECTOMY NEEDLEAdvanced Medical Products, Inc.2000-05-17550
K923995URODYNAMICS TUBING KITS #5161, #5150, #7170Advanced Medical Products, Inc.1993-04-082410
K921426ULTRA PCIAdvanced Medical Products, Inc.1992-10-051950
K912925ULTRA PVDAdvanced Medical Products, Inc.1992-06-183510
K915658SPECTRA ECGAdvanced Medical Products, Inc.1992-06-101750
K896102MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITORAdvanced Medical Products, Inc.1990-01-18870
K896103MICRO FL 7400 AMBULATORY HOLTER/BP MONITORAdvanced Medical Products, Inc.1990-01-18870
K881905MODEL MICRO SI AMBULATORY ECG MONITORAdvanced Medical Products, Inc.1988-08-02880
K872508MODEL MICRO FD+ AMBULATORY ECG MONITORAdvanced Medical Products, Inc.1987-09-25930
K870537MODEL MICRO ST AMBULATORY ECG MONITORAdvanced Medical Products, Inc.1987-04-23730
K870538MODEL 192 PRINTERAdvanced Medical Products, Inc.1987-04-23730
K852836ADVANCED MEDICAL PRODUCTS MINI-M (TENS)Advanced Medical Products, Inc.1985-08-28570
K852837ADVANCED MEDICAL PRODUCTS DR PULSE (TENS)Advanced Medical Products, Inc.1985-08-28570
K852838ADVANCED MEDICAL PRODUCTS MES TENSAdvanced Medical Products, Inc.1985-08-28570

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