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FDA 510(k)

POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM

K-Number: K884369 · 1988-11-28

ApplicantGeneral Electric Co.
Decision Date1988-11-28
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM 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 1988-11-28 under 510(k) number K884369. 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 POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM?

POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM is a medical device that received FDA 510(k) clearance on 1988-11-28. The listed applicant is General Electric Co.. The 510(k) number is K884369.

When did POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM receive FDA 510(k) clearance?

POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM received FDA 510(k) clearance on 1988-11-28, under 510(k) number K884369.

Who is the listed applicant for POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM?

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 POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM?

The FDA product code for POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM 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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