510(k) Report

FDA applicant

Pascall Saringia Medical Corp.

Cocoa Beach, FL1 decision1990–19900 recalls

FDA records 1 decision for Pascall Saringia Medical Corp. (Cocoa Beach, FL) in 1990: 1 510(k) clearance. All are in product code FPA (Set, Administration, Intravascular). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Pascall Saringia Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pascall Saringia Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pascall Saringia Medical Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Pascall”

FDA records each applicant name separately; these may or may not be the same firm.