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FDA 510(k)

SHOULDER TRANSMIT AND RECEIVE COILS

K-Number: K884603 · 1988-11-30

ApplicantDiasonics, Inc.
Decision Date1988-11-30
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHOULDER TRANSMIT AND RECEIVE COILS is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1988-11-30 under 510(k) number K884603. 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 SHOULDER TRANSMIT AND RECEIVE COILS?

SHOULDER TRANSMIT AND RECEIVE COILS is a medical device that received FDA 510(k) clearance on 1988-11-30. The listed applicant is Diasonics, Inc.. The 510(k) number is K884603.

When did SHOULDER TRANSMIT AND RECEIVE COILS receive FDA 510(k) clearance?

SHOULDER TRANSMIT AND RECEIVE COILS received FDA 510(k) clearance on 1988-11-30, under 510(k) number K884603.

Who is the listed applicant for SHOULDER TRANSMIT AND RECEIVE COILS?

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

What is the FDA product code for SHOULDER TRANSMIT AND RECEIVE COILS?

The FDA product code for SHOULDER TRANSMIT AND RECEIVE COILS 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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