510(k) Report

FDA applicant

Anesthetic Gas Reclamation, LLC

Nashville, TN2 decisions2006–20200 recalls

FDA records 2 decisions for Anesthetic Gas Reclamation, LLC (Nashville, TN) from 2006 to 2020: 2 510(k) clearances. All are in product code CBN (Apparatus, Gas-Scavenging). Its devices cite 2 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Anesthetic Gas Reclamation, Inc.”.

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 Anesthetic Gas Reclamation, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020: 1
2007high 1 (2020) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Anesthetic Gas Reclamation, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Anesthetic Gas Reclamation, LLC’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 “Anesthetic”

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