DEVON STANDARD SYRINGE, HYPODERMIC NEEDLE AND INSULIN SYRINGE— 510(k) K052551

Substantially Equivalent

Devon Safety Products, Inc.

FDA 510(k) clearance K052551 for DEVON STANDARD SYRINGE, HYPODERMIC NEEDLE AND INSULIN SYRINGE, Substantially Equivalent on 2005-09-30. Applicant: Devon Safety Products, Inc..

Clearance details

Applicant: Devon Safety Products, Inc.
Product code: Code FMF
Advisory panel: General Hospital
Date received: 2005-09-16
Decision date: 2005-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: King Of Prussia, PA, US

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Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

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.