Peter Lazic GmbH
Peter Lazic GmbH holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2019, with 5 FDA device recalls on record.
Top product codes for Peter Lazic GmbH
FDA recalls by Peter Lazic GmbH
- Z-1278-2024 — D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
- Z-1279-2024 — D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
- Z-1277-2024 — D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.
- Z-1287-2024 — L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile
- Z-1288-2024 — L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Peter Lazic GmbH
Data sourced from openFDA. This site is unofficial and independent of the FDA.