PREMVIA— 510(k) K134037

Substantially Equivalent

Biotime, Inc.

FDA 510(k) clearance K134037 for PREMVIA, Substantially Equivalent on 2014-08-07. Applicant: Biotime, Inc..

Clearance details

Applicant: Biotime, Inc.
Product code: Code KGN
Advisory panel: Unknown
Date received: 2013-12-31
Decision date: 2014-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KGN

product code KGN

Other: 2
Total: 2

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.