NERVE STIMULATOR MODEL AA 1050— 510(k) K811614

Substantially Equivalent

Anesthesia Assoc., Inc.

FDA 510(k) clearance K811614 for NERVE STIMULATOR MODEL AA 1050, Substantially Equivalent on 1981-06-18. Applicant: Anesthesia Assoc., Inc..

Clearance details

Applicant: Anesthesia Assoc., Inc.
Product code: Code BXN
Advisory panel: Anesthesiology
Date received: 1981-06-08
Decision date: 1981-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code BXN

product code BXN

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.