CURITY NERVE BLOCK TRAY

Anesthesia Conduction Kit

KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH

The following data is part of a premarket notification filed by Kendall Healthcare Products Co. Div.of Tyco Health with the FDA for Curity Nerve Block Tray.

Pre-market Notification Details

Device IDK903887
510k NumberK903887
Device Name:CURITY NERVE BLOCK TRAY
ClassificationAnesthesia Conduction Kit
Applicant KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH 15 HAMPSHIRE ST. Mansfield,  MA  02048
ContactJohn J Vozella
CorrespondentJohn J Vozella
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH 15 HAMPSHIRE ST. Mansfield,  MA  02048
Product CodeCAZ  
CFR Regulation Number868.5140 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-08-22
Decision Date1990-11-30

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