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FDA 510(k)

VITALOG PMS-8 (MODIFICATION)

K-Number: K871813 · 1987-11-23

ApplicantVitalog Corp.
Decision Date1987-11-23
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VITALOG PMS-8 (MODIFICATION) is the device name listed in this FDA 510(k) record. The listed applicant is Vitalog Corp.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K871813. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALOG PMS-8 (MODIFICATION)?

VITALOG PMS-8 (MODIFICATION) is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Vitalog Corp.. The 510(k) number is K871813.

When did VITALOG PMS-8 (MODIFICATION) receive FDA 510(k) clearance?

VITALOG PMS-8 (MODIFICATION) received FDA 510(k) clearance on 1987-11-23, under 510(k) number K871813.

Who is the listed applicant for VITALOG PMS-8 (MODIFICATION)?

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

What is the FDA product code for VITALOG PMS-8 (MODIFICATION)?

The FDA product code for VITALOG PMS-8 (MODIFICATION) is BZQ.

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.

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Other records listing Vitalog 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.

K874198VITALOG HMS-3000K845051VITALOG PMS-8K812739VITALOG PMS-8 MONITOR

Related Devices (Code: BZQ)

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.

K253274BedDot (G1)Intelligent Dots, LLCK251326Respiration Rate algorithmEdwards Lifesciences, LLCK250093Linshom Continuous Predictive Respiratory Monitoring System (CPRMS)Linshom Medical, Inc.K250934Respiree Cardio- Respiratory Monitor SystemRespiree Pte, Ltd.K243183RTMsense Respiratory Monitoring SystemRtm Vital Signs, LLCK243966FaceHeart Vitals Software Development Kit (FH vitals SDK-RR)Faceheart Corp.

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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