PERI-K PAD COLD PACK— 510(k) K920760

Substantially Equivalent

Baxter Healthcare Corp

FDA 510(k) clearance K920760 for PERI-K PAD COLD PACK, Substantially Equivalent on 1993-07-29. Applicant: Baxter Healthcare Corp.

Clearance details

Applicant: Baxter Healthcare Corp
Product code: Code IMD
Advisory panel: Physical Medicine
Date received: 1992-02-19
Decision date: 1993-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valencia, CA, US

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Adverse events under product code IMD

product code IMD

Death: 3
Injury: 600
Total: 603

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.