HOPER PTCA BALLOON CATHETER— 510(k) K123473

Substantially Equivalent

Lepu Medical Technology (Beijing) Co., Ltd.

FDA 510(k) clearance K123473 for HOPER PTCA BALLOON CATHETER, Substantially Equivalent on 2013-08-13. Applicant: Lepu Medical Technology (Beijing) Co., Ltd.. Device class: 2.

Clearance details

Applicant
Lepu Medical Technology (Beijing) Co., Ltd.
Product code
Code LOX
Device class
Class 2
Regulation
21 CFR 870.5100
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
South Euclid, OH, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code LOX

product code LOX
Death
190
Injury
1,498
Malfunction
9,670
Total
11,358

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 →

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