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FDA 510(k)

TOSHIBA 3T 32CH HEAD SPEEDER COIL,

K-Number: K122638 · 2012-09-25

Decision Date2012-09-25
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TOSHIBA 3T 32CH HEAD SPEEDER COIL, is the device name listed in this FDA 510(k) record. The listed applicant is Quality Electrodynamics. It received FDA 510(k) clearance on 2012-09-25 under 510(k) number K122638. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOSHIBA 3T 32CH HEAD SPEEDER COIL,?

TOSHIBA 3T 32CH HEAD SPEEDER COIL, is a medical device that received FDA 510(k) clearance on 2012-09-25. The listed applicant is Quality Electrodynamics. The 510(k) number is K122638.

When did TOSHIBA 3T 32CH HEAD SPEEDER COIL, receive FDA 510(k) clearance?

TOSHIBA 3T 32CH HEAD SPEEDER COIL, received FDA 510(k) clearance on 2012-09-25, under 510(k) number K122638.

Who is the listed applicant for TOSHIBA 3T 32CH HEAD SPEEDER COIL,?

The FDA 510(k) record lists Quality Electrodynamics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOSHIBA 3T 32CH HEAD SPEEDER COIL,?

The FDA product code for TOSHIBA 3T 32CH HEAD SPEEDER COIL, is MOS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Quality Electrodynamics as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 13 devices →

Related Devices (Code: MOS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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