Tem 3002G- HN Dual Tune Head Coil

FDA 510(k) K080820 · Mr Instruments, Inc.

Substantially Equivalent

510(k) numberK080820

Submission

Device name
Tem 3002G- HN Dual Tune Head Coil
Applicant
Mr Instruments, Inc.
Minnetonka, MN, US
Received
March 24, 2008
Decision date
April 2, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
MOS – Coil, Magnetic Resonance, Specialty
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1000
Specialty
Radiology

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K072931MC 3003G-32R Head CoilMOS · Traditional 10/30/2007SE
K052200Tem 3000 Head CoilMOS · Traditional 08/19/2005SE
K040937Tem 3000 Head CoilMOS · Traditional 04/23/2004SE

Questions and answers

When was Tem 3002G- HN Dual Tune Head Coil cleared by the FDA?

Tem 3002G- HN Dual Tune Head Coil (K080820) received a 510(k) decision of Substantially Equivalent on April 2, 2008, 9 days after the submission was received.

What is the product code of K080820?

The FDA product code is MOS – Coil, Magnetic Resonance, Specialty, a Class II (moderate risk) device regulated under 21 CFR 892.1000.