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FDA 510(k)

40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE

K-Number: K913325 · 1991-11-01

ApplicantResonex, Inc.
Decision Date1991-11-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE is the device name listed in this FDA 510(k) record. The listed applicant is Resonex, Inc.. It received FDA 510(k) clearance on 1991-11-01 under 510(k) number K913325. 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 40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE?

40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE is a medical device that received FDA 510(k) clearance on 1991-11-01. The listed applicant is Resonex, Inc.. The 510(k) number is K913325.

When did 40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE receive FDA 510(k) clearance?

40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE received FDA 510(k) clearance on 1991-11-01, under 510(k) number K913325.

Who is the listed applicant for 40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE?

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

What is the FDA product code for 40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE?

The FDA product code for 40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE is LNH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Resonex, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 21 devices →

Related Devices (Code: LNH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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