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SPROTTE® STANDARD (LUER/ NRFit®) Anesthesiology

PAJUNK GmbH Medizintechnologie · Class II · Cleared Nov 22, 2024

K-numberK241953
Device nameSPROTTE® STANDARD (LUER/ NRFit®) Anesthesiology
ApplicantPAJUNK GmbH Medizintechnologie
Product codeBSP
Device classClass II
Decision dateNov 22, 2024
DecisionSubstantially Equivalent
Regulation868.5150
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View the full FDA submission: accessdata.fda.gov

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