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

Applied Medical Research — Predicate Candidate Screening

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

21 daysmedian FDA review time

77 days90th percentile

22clearances measured

K-number	Device	Applicant	Decided	Review days
K800025	DINAMAP RESEARCH MONITOR 1245	Applied Medical Research	1980-02-01	25
K791580	CEREBRAL FUNCTION MONITOR 870	Applied Medical Research	1979-09-04	18
K791159	DINAMAP MODEL 855	Applied Medical Research	1979-07-30	39
K790322	OPTIONAL ACCESSORY FOOT SWITCH MODEL 100	Applied Medical Research	1979-05-14	88
K790328	MODEL 1051, MONITOR	Applied Medical Research	1979-03-02	14
K782073	DINAMAP MODELS 1160 AND 1165	Applied Medical Research	1979-02-23	72
K781064	DINAMAP MODEL 848	Applied Medical Research	1978-09-07	73
K781053	DINAMAP MODEL 846	Applied Medical Research	1978-09-07	77
K781311	ELECTRODE, NEEDLE, CFM	Applied Medical Research	1978-08-21	21
K780754	NEONATAL MONITOR	Applied Medical Research	1978-06-14	36
K780759	MODEL 902 STAND	Applied Medical Research	1978-05-19	11
K780358	ACCES. ANALOG OUTPUT ADAPTOR MODEL 910	Applied Medical Research	1978-04-28	53
K780127	DINAMAP MODEL 850	Applied Medical Research	1978-01-31	7
K780128	BLOOD PRESSURE MONITOR, ARTERIAL	Applied Medical Research	1978-01-31	7
K771981	MINIMAP MODEL 810	Applied Medical Research	1978-01-24	98
K771932	RECORDER, DINMAP, MODEL 950	Applied Medical Research	1977-11-07	24
K771931	MONITOR, DINMAP, MODEL 850	Applied Medical Research	1977-10-27	13
K771897	DINAMAP MODEL 837	Applied Medical Research	1977-10-25	19
K771895	DINAMAP MADEL 845	Applied Medical Research	1977-10-25	19
K771896	DINAMAP MODEL 835	Applied Medical Research	1977-10-25	19
K771782	DINIMAP MODEL 827A	Applied Medical Research	1977-10-04	11
K771772	DINAMAP MODEL 825A	Applied Medical Research	1977-10-04	15

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