HARMAC TEMPORARY PACING CATHETER WITH BALLOON— 510(k) K962833

Substantially Equivalent

Harmac Medical Products, Inc.

FDA 510(k) clearance K962833 for HARMAC TEMPORARY PACING CATHETER WITH BALLOON, Substantially Equivalent on 1997-10-15. Applicant: Harmac Medical Products, Inc.. Device class: 2.

Clearance details

Applicant
Harmac Medical Products, Inc.
Product code
Code LDF
Device class
Class 2
Regulation
21 CFR 870.3680
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Buffalo, NY, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code LDF

product code LDF
Death
19
Injury
188
Malfunction
694
Other
1
Total
902

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.