FDA applicant

Salt Creek Medical Technologies

Canfield, OH8 decisions1986–19870 recalls

FDA records 8 decisions for Salt Creek Medical Technologies (Canfield, OH) from 1986 to 1987: 8 510(k) clearances. Most are in product codes FPK (Tubing, Fluid Delivery) and HFW (Clamp, Umbilical). 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 Salt Creek Medical Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Salt Creek Medical Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Salt Creek Medical Technologies

Which product codes does it file in?

What has FDA decided for it lately?