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

Robert R. Moore — Predicate Candidate Screening

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

20 daysmedian FDA review time

71 days90th percentile

5clearances measured

K-number	Device	Applicant	Decided	Review days
K770658	EXERCISER, LEG, LOWER EXTREMITY	Robert R. Moore	1977-06-17	71
K770501	KNEE CUFF FOR EXPRESSING FLUID	Robert R. Moore	1977-04-05	21
K770223	HEAVY FOAM HEEL & ELBOW PROTECTORS	Robert R. Moore	1977-02-23	20
K770060	X-RAY POSITIONING DEVICE	Robert R. Moore	1977-01-24	13
K770059	ORTHOPEDIC SPECIALTIES	Robert R. Moore	1977-01-14	3

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