HI-TORQUE WHISPER LS; HI-TORQUE WHISPER MS; HI-TORQUE WHISPER MS CS-J; HI-TORQUE WHISPER ES; HI-TORQUE WHISPER ES CS-J— 510(k) K023300

Substantially Equivalent

Guidant Corp.

FDA 510(k) clearance K023300 for HI-TORQUE WHISPER LS; HI-TORQUE WHISPER MS; HI-TORQUE WHISPER MS CS-J; HI-TORQUE WHISPER ES; HI-TORQUE WHISPER ES CS-J, Substantially Equivalent on 2002-10-28. Applicant: Guidant Corp..

Clearance details

Applicant: Guidant Corp.
Product code: Code DQX
Advisory panel: Cardiovascular
Date received: 2002-10-03
Decision date: 2002-10-28
Decision: Substantially Equivalent
Clearance type: Special
Location: St Paul, MN, US

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Adverse events under product code DQX

product code DQX

Death: 298
Injury: 4,385
Malfunction: 7,203
Other: 5
Total: 11,891

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.