Cleared Traditional

K132899 - EQUASHIELD CLOSED SYSTEM DRUG TRANSFER DEVICE (CSTD) (FDA 510(k) Clearance)

May 2014
Decision
239d
Days
Class 2
Risk

K132899 is an FDA 510(k) clearance for the EQUASHIELD CLOSED SYSTEM DRUG TRANSFER DEVICE (CSTD). This device is classified as a Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System (Class II - Special Controls, product code ONB).

Submitted by Equashield Medical , Ltd. (Monroe, US). The FDA issued a Cleared decision on May 13, 2014, 239 days after receiving the submission on September 16, 2013.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.5440. Reconstitute And Transfer Antineoplastic And Other Hazardous Drugs In Healthcare Setting Indicated To Reduce Exposure Of Healthcare Personnel To Chemotherapy Agents In Healthcare Setting..

Submission Details

510(k) Number K132899 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 16, 2013
Decision Date May 13, 2014
Days to Decision 239 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code ONB - Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System
Device Class Class II - Special Controls
CFR Regulation 21 CFR 880.5440
Definition Reconstitute And Transfer Antineoplastic And Other Hazardous Drugs In Healthcare Setting Indicated To Reduce Exposure Of Healthcare Personnel To Chemotherapy Agents In Healthcare Setting.

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