PAJUNK GmbH Medizintechnologie - FDA 510(k) Cleared Devices
44
Total
44
Cleared
0
Denied
FDA 510(k) cleared devices by PAJUNK GmbH Medizintechnologie Anesthesiology ✕
27 devices
Cleared
Jul 01, 2025
SonoMSK
Anesthesiology
214d
Cleared
Jun 27, 2025
SonoPlex STIM
Anesthesiology
210d
Cleared
Jun 25, 2025
SPROTTE® STANDARD (LUER/ NRFit®) Lumbar Puncture
Anesthesiology
103d
Cleared
Mar 24, 2025
SonoTAP and SonoTAP II
Anesthesiology
130d
Cleared
Nov 22, 2024
SPROTTE® STANDARD (LUER/ NRFit®) Anesthesiology
Anesthesiology
142d
Cleared
Sep 11, 2024
SonoBlock
Anesthesiology
70d
Cleared
Dec 29, 2020
E-Cath STIM acc. Tsui
Anesthesiology
104d
Cleared
Jun 17, 2019
Epidural MiniFilter LUER 80369-7, Epidural MiniFilter NRFit 80369-6
Anesthesiology
94d
Cleared
May 16, 2019
VPC
Anesthesiology
91d
Cleared
May 03, 2018
Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7
Anesthesiology
231d
Cleared
Jul 12, 2017
NerveGuard NRFit, NerveGuard LUER
Anesthesiology
149d
Cleared
Jan 06, 2017
MultiStim ECO
Anesthesiology
163d