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FDA 510(k)

LA MONT VIDEO PATIENT MONITORING SYSTEM

K-Number: K921485 · 1992-10-22

ApplicantMedical Systems Corp.
Decision Date1992-10-22
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LA MONT VIDEO PATIENT MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Systems Corp.. It received FDA 510(k) clearance on 1992-10-22 under 510(k) number K921485. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LA MONT VIDEO PATIENT MONITORING SYSTEM?

LA MONT VIDEO PATIENT MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1992-10-22. The listed applicant is Medical Systems Corp.. The 510(k) number is K921485.

When did LA MONT VIDEO PATIENT MONITORING SYSTEM receive FDA 510(k) clearance?

LA MONT VIDEO PATIENT MONITORING SYSTEM received FDA 510(k) clearance on 1992-10-22, under 510(k) number K921485.

Who is the listed applicant for LA MONT VIDEO PATIENT MONITORING SYSTEM?

The FDA 510(k) record lists Medical Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LA MONT VIDEO PATIENT MONITORING SYSTEM?

The FDA product code for LA MONT VIDEO PATIENT MONITORING SYSTEM is GWQ.

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Other records listing Medical Systems Corp. 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.

K931736M-FLEX 5000 C3PMDK921513SPIROLITE MODEL MSC-201 SPIROMETERK904353CARDIOMATIC MODEL MSC-2001K903501RADIANT TEMPERATUR INDICATOR MODEL 25EK902192MODEL MSC SA02-5000 PULSE OXIMETERK902608CARDIOMATIC MODEL MSC-1001

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Related Devices (Code: GWQ)

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.

K261604Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32)Neuroelectrics Barcelona S.L.U.K260455New Wave SystemZeto, Inc.K233403Flexset SystemZeto, Inc.K231366Neuronaute PlusBioserenity SasK221959Q21Neurofield, Inc.K231457SPARK ScanSpark Neuro, Inc.

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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