FDA applicant
Cygnus of South Florida, Inc.
FDA records 2 decisions for Cygnus of South Florida, Inc. (Hollywood, FL) in 1986: 2 510(k) clearances. Most are in product codes JQP (Calculator/Data Processing Module, For…) and DQK (Computer, Diagnostic, Programmable). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Cygnus of South Florida, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Cygnus of South Florida, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Cygnus of South Florida, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Cygnus”
FDA records each applicant name separately; these may or may not be the same firm.