BALLARD MEDICAL PRODUCTS EPIDURAL AND SPINAL NEEDLES— 510(k) K000495

Name: FDA 510(k) clearance K000495
Creator: U.S. Food and Drug Administration
Published: 2000-03-28

Substantially Equivalent

Ballard Medical Products

FDA 510(k) clearance K000495 for BALLARD MEDICAL PRODUCTS EPIDURAL AND SPINAL NEEDLES, Substantially Equivalent on 2000-03-28. Applicant: Ballard Medical Products. Device class: 2.

Clearance details

Applicant: Ballard Medical Products
Product code: Code BSP
Device class: Class 2
Regulation: 21 CFR 868.5150
Advisory panel: Anesthesiology
Date received: 2000-02-15
Decision date: 2000-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Draper, UT, US

Download summary PDF View on FDA.gov ↗

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K993138 — BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT1999-10-20
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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.