FDA applicant

Anesthesia Assoc., Inc.

Walker, MI3 decisions1981–19920 recalls

FDA records 3 decisions for Anesthesia Assoc., Inc. (Walker, MI) from 1981 to 1992: 3 510(k) clearances. Most are in product codes CAI (Circuit, Breathing (W Connector, Adaptor, Y…) and BXN (Stimulator, Nerve, Battery-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, anesthesiology panel, where it files most

How often FDA has decided Anesthesia Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anesthesia Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Anesthesia”

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

Anesthesia Safety Products, LLC 1 Anesthesia Respiratory Technology, Inc. 1

Anesthesia Assoc., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Anesthesia”