CV PERI-GUARD AND VASCU-GUARD— 510(k) K983602

Substantially Equivalent

Bio-Vascular, Inc.

FDA 510(k) clearance K983602 for CV PERI-GUARD AND VASCU-GUARD, Substantially Equivalent on 1998-11-12. Applicant: Bio-Vascular, Inc.. Device class: 2.

Clearance details

Applicant
Bio-Vascular, Inc.
Product code
Code DXZ
Device class
Class 2
Regulation
21 CFR 870.3470
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
St. Paul, MN, US
Download summary PDFView on FDA.gov ↗

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More clearances from Bio-Vascular, Inc.

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Adverse events under product code DXZ

product code DXZ
Death
19
Injury
265
Total
284

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 K983602

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 K983602.

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