STIMULATOR, BATTERY POWERED— 510(k) K790123

Substantially Equivalent

Intermedics, Inc.

FDA 510(k) clearance K790123 for STIMULATOR, BATTERY POWERED, Substantially Equivalent on 1979-02-06. Applicant: Intermedics, Inc..

Clearance details

Applicant: Intermedics, Inc.
Product code: Code BXN
Advisory panel: Anesthesiology
Date received: 1979-01-23
Decision date: 1979-02-06
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.