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FDA 510(k)

NEUROMUSCULAR TRANSMISSION MONITOR

K-Number: K905092 · 1991-06-25

Decision Date1991-06-25
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEUROMUSCULAR TRANSMISSION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Utah Medical Products, Inc.. It received FDA 510(k) clearance on 1991-06-25 under 510(k) number K905092. The device is classified under product code BXN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROMUSCULAR TRANSMISSION MONITOR?

NEUROMUSCULAR TRANSMISSION MONITOR is a medical device that received FDA 510(k) clearance on 1991-06-25. The listed applicant is Utah Medical Products, Inc.. The 510(k) number is K905092.

When did NEUROMUSCULAR TRANSMISSION MONITOR receive FDA 510(k) clearance?

NEUROMUSCULAR TRANSMISSION MONITOR received FDA 510(k) clearance on 1991-06-25, under 510(k) number K905092.

Who is the listed applicant for NEUROMUSCULAR TRANSMISSION MONITOR?

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

What is the FDA product code for NEUROMUSCULAR TRANSMISSION MONITOR?

The FDA product code for NEUROMUSCULAR TRANSMISSION MONITOR is BXN.

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 Utah Medical Products, 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 37 devices →

Related Devices (Code: BXN)

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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