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FDA 510(k)

SIGNA PROFILE SMALL HEAD COIL

K-Number: K982972 · 1998-11-16

ApplicantGE Medical Systems
Decision Date1998-11-16
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIGNA PROFILE SMALL HEAD COIL is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 1998-11-16 under 510(k) number K982972. 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 SIGNA PROFILE SMALL HEAD COIL?

SIGNA PROFILE SMALL HEAD COIL is a medical device that received FDA 510(k) clearance on 1998-11-16. The listed applicant is GE Medical Systems. The 510(k) number is K982972.

When did SIGNA PROFILE SMALL HEAD COIL receive FDA 510(k) clearance?

SIGNA PROFILE SMALL HEAD COIL received FDA 510(k) clearance on 1998-11-16, under 510(k) number K982972.

Who is the listed applicant for SIGNA PROFILE SMALL HEAD COIL?

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

What is the FDA product code for SIGNA PROFILE SMALL HEAD COIL?

The FDA product code for SIGNA PROFILE SMALL HEAD COIL is MOS.

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Related Devices (Code: MOS)

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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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