Cospan Pediatric Continuous Spinal Anesthesia Tray

FDA 510(k) K902312 · Kendall Healthcare Products Co. Div.Of Tyco Health

Substantially Equivalent

510(k) numberK902312

Submission

Device name
Cospan Pediatric Continuous Spinal Anesthesia Tray
Applicant
Kendall Healthcare Products Co. Div.Of Tyco Health
Salt Lake City, UT, US
Received
May 23, 1990
Decision date
July 30, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CAZ – Anesthesia Conduction Kit
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5140
Specialty
Anesthesiology

This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

Other 510(k)s with product code CAZ

510(k)DeviceApplicantDecision
K222341Arrow 0.2 Micron Flat Filter, GVSCAZ · Traditional Arrow International, LLC02/13/2023SE
K210983BD Epilor SyringeCAZ · Traditional Becton, Dickinson and Company05/19/2022SE
K201356Plastic LOR SyringeCAZ · Traditional Jiangsu Caina Medical Co.,Ltd02/12/2021SE
K202699E-Cath STIM acc. TsuiCAZ · Special PAJUNK GmbH Medizintechnologie12/29/2020SE
K190345VPCCAZ · Traditional PAJUNK GmbH Medizintechnologie05/16/2019SE
K161075Arrow Epidural Catheter KitCAZ · Traditional Teleflexmedical, Inc.10/04/2016SE
K153652ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/SetCAZ · Traditional Teleflex, Inc.06/21/2016SE
K143581Arrow Epidural Catheter KitCAZ · Traditional Teleflexmedical, Inc.06/26/2015SE
K122690Ultraquik Peripheral Nerve Block NeedleCAZ · Traditional Arrow International, Inc.12/21/2012SE
K110053Correctinject Safety System, Catheter Connector, Filter, Infusion Adaptor, Syringe KitCAZ · Traditional Smiths Medical Asd, Inc.09/14/2012SE

More from Smiths Medical Asd, Inc.

510(k)DeviceDecision
K973763Kendall Curity Iodoform Packing StripEFQ · Traditional 12/31/1997SE
K973511Kendall Curity Petrolatum GauzeFRO · Traditional 12/16/1997SN
K973507Kendall Xeroform Petrolatum Dressing (6311,6312,6313,6314,6315,6316,6317)FRO · Traditional 12/15/1997SN
K973619Kendall Curity Non-Adhering DressingKMF · Traditional 12/10/1997SN
K973509Kendall Curasorb ZN + MG Alginate Wound DressingKMF · Traditional 12/04/1997SN
K973546Kendall Fast-Cath Pre Lubricated Urethral CatheterEZD · Traditional 11/07/1997SE
K970266Kendall Hydrophilic Powder Wound DressingKGN · Traditional 04/23/1997SN
K963446Kendall Dual Lumen CatheterMPB · Traditional 03/18/1997SE
K964899Kendall Curity Ureteral CatheterEYB · Traditional 02/07/1997SE
K964519Curity Thoracentesis TrayGCX · Traditional 12/20/1996SE

Questions and answers

When was Cospan Pediatric Continuous Spinal Anesthesia Tray cleared by the FDA?

Cospan Pediatric Continuous Spinal Anesthesia Tray (K902312) received a 510(k) decision of Substantially Equivalent on July 30, 1990, 68 days after the submission was received.

What is the product code of K902312?

The FDA product code is CAZ – Anesthesia Conduction Kit, a Class II (moderate risk) device regulated under 21 CFR 868.5140.