LEAD INTRODUCER SET, VARIOUS MODELS AND SIZES— 510(k) K931662

Substantially Equivalent

Pace Medical

FDA 510(k) clearance K931662 for LEAD INTRODUCER SET, VARIOUS MODELS AND SIZES, Substantially Equivalent on 1993-08-31. Applicant: Pace Medical. Device class: 2.

Clearance details

Applicant
Pace Medical
Product code
Code DYB
Device class
Class 2
Regulation
21 CFR 870.1340
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Waltham, MA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code DYB

product code DYB
Death
808
Injury
5,922
Malfunction
16,516
Other
5
Total
23,251

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.