PERCUTANEOUS GRAINAGE CATHETER— 510(k) K943893

Substantially Equivalent

Menlo Care, Inc.

FDA 510(k) clearance K943893 for PERCUTANEOUS GRAINAGE CATHETER, Substantially Equivalent on 1995-03-07. Applicant: Menlo Care, Inc..

Clearance details

Applicant: Menlo Care, Inc.
Product code: Code LJE
Advisory panel: Unknown
Date received: 1994-08-09
Decision date: 1995-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, CA, US

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Adverse events under product code LJE

product code LJE

Death: 6
Total: 6

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.