C-Flex Medical Grade Tubing

FDA 510(k) K833076 · Concept, Inc.

Substantially Equivalent

510(k) numberK833076

Submission

Device name
C-Flex Medical Grade Tubing
Applicant
Concept, Inc.
Mchenry, IL, US
Received
September 9, 1983
Decision date
November 21, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FPK – Tubing, Fluid Delivery
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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Questions and answers

When was C-Flex Medical Grade Tubing cleared by the FDA?

C-Flex Medical Grade Tubing (K833076) received a 510(k) decision of Substantially Equivalent on November 21, 1983, 73 days after the submission was received.

What is the product code of K833076?

The FDA product code is FPK – Tubing, Fluid Delivery, a Class II (moderate risk) device regulated under 21 CFR 880.5440.