RNS Arthrogram Tray

FDA 510(k) K962040 · Contour Fabricators of Florida, Inc.

Substantially Equivalent

510(k) numberK962040

Submission

Device name
RNS Arthrogram Tray
Applicant
Contour Fabricators of Florida, Inc.
Tarpon Springs, FL, US
Received
May 24, 1996
Decision date
June 25, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FMI – Needle, Hypodermic, Single Lumen
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5570
Specialty
General Hospital

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More from Ningbo Medsun Medical Co., Ltd.

510(k)DeviceDecision
K955685RNS Sterile, Disposable CT Biopsy TrayDXT · Traditional 10/04/1996SE
K955687RNS Sterile, Disposable Radiographic Contrast TrayJAA · Traditional 06/03/1996SE
K955689RNS Sterile, Disposable Digital Angiographic TrayDWS · Traditional 05/15/1996SE
K955684RNS Sterile, Disposable Angiographic TrayDXT · Traditional 05/02/1996SESK
K955679RNS Sterile, Disposable Amniocentesis TrayHIO · Traditional 03/12/1996SE
K955688RNS Sterile, Disposable Standard Biopsy TrayFRG · Traditional 02/21/1996SE
K955686RNS, Sterile Disposable Percutaneous Cholangiographic TrayFRG · Traditional 02/21/1996SE
K955678RNS Sterile Disposable Puncture TrayFRG · Traditional 02/21/1996SE
K955683RNS Sterile, Disposable Breast Biopsy/Localization TrayMJG · Traditional 02/01/1996SE
K952396Redi Nurse System (RNS) Sterile 0.9% Sodium Chloride SolutionBSY · Traditional 08/15/1995SE

Questions and answers

When was RNS Arthrogram Tray cleared by the FDA?

RNS Arthrogram Tray (K962040) received a 510(k) decision of Substantially Equivalent on June 25, 1996, 32 days after the submission was received.

What is the product code of K962040?

The FDA product code is FMI – Needle, Hypodermic, Single Lumen, a Class II (moderate risk) device regulated under 21 CFR 880.5570.