510(k) Report

FDA applicant

Crystal Medical Products, Inc.

Barrington, IL5 decisions1984–19860 recalls

FDA records 5 decisions for Crystal Medical Products, Inc. (Barrington, IL) from 1984 to 1986: 5 510(k) clearances. Most are in product codes HGX (Pump, Breast, Powered) and HGY (Pump, Breast, Non-Powered). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Crystal 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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Other applicant names beginning “Crystal”

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