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

Viggo Products — Predicate Candidate Screening

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

78 daysmedian FDA review time

93 days90th percentile

7clearances measured

K-number	Device	Applicant	Decided	Review days
K850769	VIGGO ACCESSORIES FOR I.V. THERAPY	Viggo Products	1985-05-29	93
K850276	VIGGO NEOFLON INFUSION CANNULA	Viggo Products	1985-04-12	79
K850277	VIGGO I.V. ACCESSORIES-VIGGO EXTENSION TUBES ETC.	Viggo Products	1985-04-12	79
K850460	VIGGO SECALON T CATHETER	Viggo Products	1985-04-11	64
K850280	VIGGO CONNECTA 3-WAY INFUSION STOPCOCK	Viggo Products	1985-04-11	78
K850278	VASCULON I.V. CANNULAE	Viggo Products	1985-04-09	76
K850349	VIGGO ARTERIAL CANNULA	Viggo Products	1985-04-09	71

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