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FDA 510(k)

CP HEAD COIL & 260MM (CV) TRANSMIT-RECEIVE COIL

K-Number: K883872 · 1988-11-21

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1988-11-21
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CP HEAD COIL & 260MM (CV) TRANSMIT-RECEIVE COIL is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1988-11-21 under 510(k) number K883872. 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 CP HEAD COIL & 260MM (CV) TRANSMIT-RECEIVE COIL?

CP HEAD COIL & 260MM (CV) TRANSMIT-RECEIVE COIL is a medical device that received FDA 510(k) clearance on 1988-11-21. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K883872.

When did CP HEAD COIL & 260MM (CV) TRANSMIT-RECEIVE COIL receive FDA 510(k) clearance?

CP HEAD COIL & 260MM (CV) TRANSMIT-RECEIVE COIL received FDA 510(k) clearance on 1988-11-21, under 510(k) number K883872.

Who is the listed applicant for CP HEAD COIL & 260MM (CV) TRANSMIT-RECEIVE COIL?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CP HEAD COIL & 260MM (CV) TRANSMIT-RECEIVE COIL?

The FDA product code for CP HEAD COIL & 260MM (CV) TRANSMIT-RECEIVE 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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