ClearanceBrief
Company ยท DE

Peter Lazic Gmbh

FDA 510(k) clearances and medical device recalls filed under this name, 2008 to 2019. Name variants (Inc, Corp, punctuation) are merged.

2510(k) clearances (0 in 12 months)
5recalls (0 in 12 months)
5recalls that name a 510(k)

Product codes

CodeDeviceRecords
HCHClip, Aneurysm4
HCIApplier, Aneurysm Clip3

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 12, 2019K180757D-Clip; D-Clip Applier
Peter Lazic GmbH, DE
HCH
Sep 25, 2008K081489L-ANEURYSM-CLIP SYSTEM & L-ANEURYSM CLIP APPLIERS, YASARGIL ANEURYSM CLIPS & YASARGIL ANEURYSM CLIP APPLIERS
Peter Lazic GmbH, DE
HCH

Latest recalls

DateFirm and productCodeLinked 510(k)
Mar 12, 2024Peter Lazic Gmbh
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
Open, Classified		 HCHK081489
Mar 12, 2024Peter Lazic Gmbh
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile
Open, Classified		 HCHK081489
Mar 11, 2024Peter Lazic Gmbh
D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
Open, Classified		 HCIK180757
Mar 11, 2024Peter Lazic Gmbh
D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
Open, Classified		 HCIK180757
Mar 11, 2024Peter Lazic Gmbh
D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.
Open, Classified		 HCIK180757
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