CONPHAR SILICONE DRAINS-STERILE— 510(k) K791254

Substantially Equivalent

Conphar, Inc.

FDA 510(k) clearance K791254 for CONPHAR SILICONE DRAINS-STERILE, Substantially Equivalent on 1979-08-03. Applicant: Conphar, Inc..

Clearance details

Applicant: Conphar, Inc.
Product code: Code KDQ
Advisory panel: General Hospital
Date received: 1979-07-06
Decision date: 1979-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KDQ

product code KDQ

Death: 8
Malfunction: 637
Total: 645

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.