FDA applicant

Phase Medical Systems, Inc.

Santa Ana, CA1 decision1988–19880 recalls

FDA records 1 decision for Phase Medical Systems, Inc. (Santa Ana, CA) in 1988: 1 510(k) clearance. All are in product code FOZ (Catheter, Intravascular, Therapeutic…). 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 Phase Medical Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Phase Medical Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Phase Medical Systems, 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) Report

Other applicant names beginning “Phase”

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

Phase-R Corp. 1 Phase Medical, Inc. 1 Phase One Medical 1 Phase One Disign Co. 1 Phase I Corp. 1 Phase Change 1

Phase Medical Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Phase”