Lollipop BiteBlock— 510(k) K200652

Substantially Equivalent

Radtec Medical Devices, Inc.

FDA 510(k) clearance K200652 for Lollipop BiteBlock, Substantially Equivalent on 2020-07-06. Applicant: Radtec Medical Devices, Inc..

Clearance details

Applicant: Radtec Medical Devices, Inc.
Product code: Code IYE
Advisory panel: Radiology
Date received: 2020-03-12
Decision date: 2020-07-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Carlos, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code IYE

product code IYE

Malfunction: 455
Other: 3
Total: 458

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.