BD PowerPiCC Catheter— 510(k) K210264

Substantially Equivalent

Bard Access Systems, Inc.

FDA 510(k) clearance K210264 for BD PowerPiCC Catheter, Substantially Equivalent on 2021-07-30. Applicant: Bard Access Systems, Inc.. Device class: 2.

Clearance details

Applicant
Bard Access Systems, Inc.
Product code
Code LJS
Device class
Class 2
Regulation
21 CFR 880.5970
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Salt Lake Ciy,, UT, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code LJS

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More clearances from Bard Access Systems, Inc.

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Adverse events under product code LJS

product code LJS
Death
31
Injury
2,791
Malfunction
18,374
Other
5
Total
21,201

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K210264

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K210264.

Data sourced from openFDA. This site is unofficial and independent of the FDA.