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FDA 510(k)

GE QUADRATURE T/L SPINE SURF COIL, M1085AP/M1285AP

K-Number: K902663 · 1990-09-20

ApplicantGeneral Electric Co.
Decision Date1990-09-20
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE QUADRATURE T/L SPINE SURF COIL, M1085AP/M1285AP 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 1990-09-20 under 510(k) number K902663. 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 GE QUADRATURE T/L SPINE SURF COIL, M1085AP/M1285AP?

GE QUADRATURE T/L SPINE SURF COIL, M1085AP/M1285AP is a medical device that received FDA 510(k) clearance on 1990-09-20. The listed applicant is General Electric Co.. The 510(k) number is K902663.

When did GE QUADRATURE T/L SPINE SURF COIL, M1085AP/M1285AP receive FDA 510(k) clearance?

GE QUADRATURE T/L SPINE SURF COIL, M1085AP/M1285AP received FDA 510(k) clearance on 1990-09-20, under 510(k) number K902663.

Who is the listed applicant for GE QUADRATURE T/L SPINE SURF COIL, M1085AP/M1285AP?

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 GE QUADRATURE T/L SPINE SURF COIL, M1085AP/M1285AP?

The FDA product code for GE QUADRATURE T/L SPINE SURF COIL, M1085AP/M1285AP 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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