MONOJECT DIAMOND POINT SPINAL NEEDLE (28G X 3 1/2)— 510(k) K951265

Substantially Equivalent

Sherwood Medical Co.

FDA 510(k) clearance K951265 for MONOJECT DIAMOND POINT SPINAL NEEDLE (28G X 3 1/2), Substantially Equivalent on 1995-04-10. Applicant: Sherwood Medical Co..

Clearance details

Applicant: Sherwood Medical Co.
Product code: Code BSP
Advisory panel: Anesthesiology
Date received: 1995-03-21
Decision date: 1995-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

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Adverse events under product code BSP

product code BSP

Death: 2
Total: 2

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.