Accu-Flo* Unitized Shunt

FDA 510(k) K904120 · Codman & Shurtleff, Inc.

Substantially Equivalent

510(k) numberK904120

Submission

Device name
Accu-Flo* Unitized Shunt
Applicant
Codman & Shurtleff, Inc.
Randolph, MA, US
Received
September 6, 1990
Decision date
October 9, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JXG – Shunt, Central Nervous System And Components
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5550
Specialty
Neurology
Implant
Yes

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Questions and answers

When was Accu-Flo* Unitized Shunt cleared by the FDA?

Accu-Flo* Unitized Shunt (K904120) received a 510(k) decision of Substantially Equivalent on October 9, 1990, 33 days after the submission was received.

What is the product code of K904120?

The FDA product code is JXG – Shunt, Central Nervous System And Components, a Class II (moderate risk) device regulated under 21 CFR 882.5550.