Stryker Antimic Catheter

FDA 510(k) K072702 · Stryker Instruments, Instruments Div.

Substantially Equivalent

510(k) numberK072702

Submission

Device name
Stryker Antimic Catheter
Applicant
Stryker Instruments, Instruments Div.
Kalamazoo, MI, US
Received
September 24, 2007
Decision date
March 19, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BSO – Catheter, Conduction, Anesthetic
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5120
Specialty
Anesthesiology

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Questions and answers

When was Stryker Antimic Catheter cleared by the FDA?

Stryker Antimic Catheter (K072702) received a 510(k) decision of Substantially Equivalent on March 19, 2008, 177 days after the submission was received.

What is the product code of K072702?

The FDA product code is BSO – Catheter, Conduction, Anesthetic, a Class II (moderate risk) device regulated under 21 CFR 868.5120.