Continuous Epidural Anesth. Kits W/Nylon Catheters

FDA 510(k) K873943 · Arrow Intl., Inc.

Substantially Equivalent

510(k) numberK873943

Submission

Device name
Continuous Epidural Anesth. Kits W/Nylon Catheters
Applicant
Arrow Intl., Inc.
Reading, PA, US
Received
September 28, 1987
Decision date
October 20, 1987
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.

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K041153Sharpsaway II Locking Disposable CupFMI · Traditional 07/12/2004SE
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Questions and answers

When was Continuous Epidural Anesth. Kits W/Nylon Catheters cleared by the FDA?

Continuous Epidural Anesth. Kits W/Nylon Catheters (K873943) received a 510(k) decision of Substantially Equivalent on October 20, 1987, 22 days after the submission was received.

What is the product code of K873943?

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