KITECKO ULTRASOUND STANDOFF PAD— 510(k) K851982

Substantially Equivalent

3M Company

FDA 510(k) clearance K851982 for KITECKO ULTRASOUND STANDOFF PAD, Substantially Equivalent on 1985-08-14. Applicant: 3M Company.

Clearance details

Applicant
3M Company
Product code
Code IYO
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Cottae Grove, MN, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code IYO

product code IYO
Malfunction
3,339
Total
3,339

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.