CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS

Anesthesia Conduction Kit

CARAPACE, INC.

The following data is part of a premarket notification filed by Carapace, Inc. with the FDA for Carapace Epidural Block & Spinal Myelogram Trays.

Pre-market Notification Details

Device IDK931670
510k NumberK931670
Device Name:CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS
ClassificationAnesthesia Conduction Kit
Applicant CARAPACE, INC. 2701 W CONCORD ST. Broken Arrow,  OK  74012
ContactJerry W Myers
CorrespondentJerry W Myers
CARAPACE, INC. 2701 W CONCORD ST. Broken Arrow,  OK  74012
Product CodeCAZ  
CFR Regulation Number868.5140 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-04-06
Decision Date1994-01-25

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