510(k) Report

FDA applicant

Rennels Medical Corp.

Morganton, NC1 decision2001–20010 recalls

FDA records 1 decision for Rennels Medical Corp. (Morganton, NC) in 2001: 1 510(k) clearance. All are in product code CAH (Filter, Bacterial, Breathing-Circuit). 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, anesthesiology panel, where it files most

How often FDA has decided Rennels Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rennels Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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