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

Atomic Products Corp. — Predicate Candidate Screening

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

78 daysmedian FDA review time

334 days90th percentile

10clearances measured

K-number	Device	Applicant	Decided	Review days
K915541	SPECT TABLE, MODEL #056-760	Atomic Products Corp.	1992-01-17	38
K913055	THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900	Atomic Products Corp.	1991-09-06	59
K904187	ECONOMY C-ARM TABLE, MODEL # 056-005	Atomic Products Corp.	1990-11-29	78
K904623	RADIOGRAPHIC TRANSPORT, TRAUMA MODEL 056-230, 235	Atomic Products Corp.	1990-11-06	26
K900851	DIGITAL IMAGE ENHANCEMENT SYSTEM	Atomic Products Corp.	1990-05-11	78
K895799	RECTILINEAR SCANNER MODEL #187-270	Atomic Products Corp.	1990-02-01	126
K884312	ATOMLAB 100, MODEL 086-250 & 200 MODEL 086-270	Atomic Products Corp.	1989-02-16	126
K871868	VENTI-SCAN II	Atomic Products Corp.	1988-04-11	334
K874332	MRI STRETCHER	Atomic Products Corp.	1988-01-05	75
K790835	DYNAJECT	Atomic Products Corp.	1979-06-22	53

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