510(k) Report

FDA applicant

Innovative Medical Products, Inc.

Hrahan, LA2 decisions1990–19920 recalls

FDA records 2 decisions for Innovative Medical Products, Inc. (Hrahan, LA) from 1990 to 1992: 2 510(k) clearances. Most are in product codes DQA (Oximeter) and HFC (Aspirator, Endocervical). 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 Innovative Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Innovative Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Innovative Medical Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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