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FDA 510(k)

MT/S CARLSON SPINE COIL, PART # 100-50082500-01

K-Number: K884604 · 1988-11-30

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

Device Summary

MT/S CARLSON SPINE COIL, PART # 100-50082500-01 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 K884604. 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 MT/S CARLSON SPINE COIL, PART # 100-50082500-01?

MT/S CARLSON SPINE COIL, PART # 100-50082500-01 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 K884604.

When did MT/S CARLSON SPINE COIL, PART # 100-50082500-01 receive FDA 510(k) clearance?

MT/S CARLSON SPINE COIL, PART # 100-50082500-01 received FDA 510(k) clearance on 1988-11-30, under 510(k) number K884604.

Who is the listed applicant for MT/S CARLSON SPINE COIL, PART # 100-50082500-01?

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 MT/S CARLSON SPINE COIL, PART # 100-50082500-01?

The FDA product code for MT/S CARLSON SPINE COIL, PART # 100-50082500-01 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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