510(k) Report

FDA applicant

Lawrence Medical Systems, Inc.

Cammarillo, CA4 decisions1985–19880 recalls

FDA records 4 decisions for Lawrence Medical Systems, Inc. (Cammarillo, CA) from 1985 to 1988: 4 510(k) clearances. Most are in product codes DPW (Flowmeter, Blood, Cardiovascular) and DXK (Echocardiograph). 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, cardiovascular panel, where it files most

How often FDA has decided Lawrence Medical Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lawrence 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 “Lawrence”

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