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FDA 510(k)

GENERAL PURPOSE FLEX COIL

K-Number: K923264 · 1992-09-30

ApplicantGeneral Electric Co.
Decision Date1992-09-30
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GENERAL PURPOSE FLEX COIL is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1992-09-30 under 510(k) number K923264. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL PURPOSE FLEX COIL?

GENERAL PURPOSE FLEX COIL is a medical device that received FDA 510(k) clearance on 1992-09-30. The listed applicant is General Electric Co.. The 510(k) number is K923264.

When did GENERAL PURPOSE FLEX COIL receive FDA 510(k) clearance?

GENERAL PURPOSE FLEX COIL received FDA 510(k) clearance on 1992-09-30, under 510(k) number K923264.

Who is the listed applicant for GENERAL PURPOSE FLEX COIL?

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

What is the FDA product code for GENERAL PURPOSE FLEX COIL?

The FDA product code for GENERAL PURPOSE FLEX COIL is LNH.

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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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