FDA 510(k) Applications Submitted by R C HALL

FDA 510(k) Number Submission Date Device Name Applicant
K960734 02/22/1996 HAEMOCELL SYSTEM 350 OR S350 HAEMOCELL PLC
K161696 06/20/2016 aap LOQTEQ« Distal Lateral Humerus Plate 2.7/3.5 AAP IMPLANTATE AG
K161703 06/20/2016 LOQTEQ Distal Fibula Plate 3.5, Cancellous Screw 4.0, Washer AAP IMPLANTATE AG
K161747 06/24/2016 LOQTEQ« VA Distal Tibia Plate System: LOQTEQ« VA Distal Medial Tibia Plate 3.5; LOQTEQ« VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ« VA Distal Fibula Plate 2.7/3.5 aap Implantate AG
K220006 01/04/2022 angioLOCK Polymer Ligating Clip A2 Medical Systems, LLC
K230966 04/05/2023 angiOCCLUDE Ligating Clips A2 Medical Systems, LLC
K993033 09/09/1999 INTRAY GC BIOMED DIAGNOSTICS, INC.
K110795 03/22/2011 V200 INTELLI-TRAK OPTION RESPIRONICS CALIFORNIA, INC.
K003472 11/08/2000 INTEGRA OXYGEN CONCENTRATORS MODEL 6400-OM SEQUAL TECHNOLOGIES, INC.
K973790 10/06/1997 ABC LINEARITY VERIFIERS SC CALIBRATORS & CONTROLS LLC.
K982217 06/24/1998 AC/AD LINEARITY VERIFIERS SC CALIBRATORS & CONTROLS LLC.
K082294 08/12/2008 WESTAR SERIES DENTAL UNITS WESTAR MEDICAL PRODUCTS, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact