FLEXCATH STEERABLE SHEATH & DILATOR, MODELS 3FC10, 3FC12— 510(k) K081049

Substantially Equivalent

Cryocath Technologies, Inc.

FDA 510(k) clearance K081049 for FLEXCATH STEERABLE SHEATH & DILATOR, MODELS 3FC10, 3FC12, Substantially Equivalent on 2008-06-27. Applicant: Cryocath Technologies, Inc..

Clearance details

Applicant: Cryocath Technologies, Inc.
Product code: Code DRA
Advisory panel: Cardiovascular
Date received: 2008-04-14
Decision date: 2008-06-27
Decision: Substantially Equivalent
Clearance type: Special
Location: Galisteo, NM, US

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Adverse events under product code DRA

product code DRA

Death: 156
Injury: 3,133
Malfunction: 6,266
Total: 9,555

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.