Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX COIL

K-Number: K123681 · 2013-02-22

Decision Date2013-02-22
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX COIL is the device name listed in this FDA 510(k) record. The listed applicant is Wipro GE Healthcare Private, Ltd.. It received FDA 510(k) clearance on 2013-02-22 under 510(k) number K123681. 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 1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX COIL?

1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX COIL is a medical device that received FDA 510(k) clearance on 2013-02-22. The listed applicant is Wipro GE Healthcare Private, Ltd.. The 510(k) number is K123681.

When did 1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX COIL receive FDA 510(k) clearance?

1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX COIL received FDA 510(k) clearance on 2013-02-22, under 510(k) number K123681.

Who is the listed applicant for 1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX COIL?

The FDA 510(k) record lists Wipro GE Healthcare Private, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX COIL?

The FDA product code for 1.5T 4CH LARGE FLEX COIL, 1.5 4CH SMALL FLEX 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 Wipro GE Healthcare Private, Ltd. 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.

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.

↑