SurBlate Ablation System— 510(k) K223272

Substantially Equivalent

Mima-Pro Scientific, Inc.

FDA 510(k) clearance K223272 for SurBlate Ablation System, Substantially Equivalent on 2023-02-28. Applicant: Mima-Pro Scientific, Inc..

Clearance details

Applicant
Mima-Pro Scientific, Inc.
Product code
Code NEY
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Richmond, CA
Download summary PDFView on FDA.gov ↗

Adverse events under product code NEY

product code NEY
Death
24
Injury
388
Malfunction
462
Other
1
Total
875

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.