ELECTRO-SURGICAL GROUNDING PAD— 510(k) K780298

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K780298 for ELECTRO-SURGICAL GROUNDING PAD, Substantially Equivalent on 1978-02-28. Applicant: Johnson & Johnson Professionals, Inc..

Clearance details

Applicant
Johnson & Johnson Professionals, Inc.
Product code
Code GEI
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Raynham, MA, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code GEI

product code GEI
Death
133
Injury
7,585
Malfunction
35,808
Other
44
Total
43,570

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.