DEVIN-NESTOR PNEUMATIC TOURNIQUET

Tourniquet, Pneumatic

NESTOR ENGINEERING ASSOCIATES, INC.

The following data is part of a premarket notification filed by Nestor Engineering Associates, Inc. with the FDA for Devin-nestor Pneumatic Tourniquet.

Pre-market Notification Details

Device IDK780988
510k NumberK780988
Device Name:DEVIN-NESTOR PNEUMATIC TOURNIQUET
ClassificationTourniquet, Pneumatic
Applicant NESTOR ENGINEERING ASSOCIATES, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKCY  
CFR Regulation Number878.5910 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1978-06-14
Decision Date1978-10-03

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