POWER PACK 350/BATTERY PACK 351— 510(k) K923992

Substantially Equivalent

Siemens Medical Solutions USA, Inc.

FDA 510(k) clearance K923992 for POWER PACK 350/BATTERY PACK 351, Substantially Equivalent on 1993-04-13. Applicant: Siemens Medical Solutions USA, Inc..

Clearance details

Applicant: Siemens Medical Solutions USA, Inc.
Product code: Code CBK
Advisory panel: Anesthesiology
Date received: 1992-08-10
Decision date: 1993-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Iselin, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code CBK

product code CBK

Death: 736
Injury: 3,628
Malfunction: 98,786
Other: 4
Total: 103,154

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.