NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER— 510(k) K952884

Name: FDA 510(k) clearance K952884
Creator: U.S. Food and Drug Administration
Published: 1996-02-21

Substantially Equivalent

Meadox Medicals, Div. Boston Scientific Corp.

FDA 510(k) clearance K952884 for NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER, Substantially Equivalent on 1996-02-21. Applicant: Meadox Medicals, Div. Boston Scientific Corp.. Device class: 2.

Clearance details

Applicant: Meadox Medicals, Div. Boston Scientific Corp.
Product code: Code LIT
Device class: Class 2
Regulation: 21 CFR 870.1250
Advisory panel: Cardiovascular
Date received: 1995-06-23
Decision date: 1996-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oakland, NJ, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LIT

product code LIT

Death: 27
Injury: 1,256
Malfunction: 12,127
Total: 13,410

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.