MINI-VOL I.V. SET

Set, Administration, Intravascular

BEECH MEDICAL, INC.

The following data is part of a premarket notification filed by Beech Medical, Inc. with the FDA for Mini-vol I.v. Set.

Pre-market Notification Details

Device IDK831088
510k NumberK831088
Device Name:MINI-VOL I.V. SET
ClassificationSet, Administration, Intravascular
Applicant BEECH MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFPA  
CFR Regulation Number880.5440 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-04-04
Decision Date1983-04-28

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