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FDA 510(k)

VITALOG PMS-8 MONITOR

K-Number: K812739 · 1981-12-29

ApplicantVitalog Corp.
Decision Date1981-12-29
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITALOG PMS-8 MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Vitalog Corp.. It received FDA 510(k) clearance on 1981-12-29 under 510(k) number K812739. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALOG PMS-8 MONITOR?

VITALOG PMS-8 MONITOR is a medical device that received FDA 510(k) clearance on 1981-12-29. The listed applicant is Vitalog Corp.. The 510(k) number is K812739.

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

VITALOG PMS-8 MONITOR received FDA 510(k) clearance on 1981-12-29, under 510(k) number K812739.

Who is the listed applicant for VITALOG PMS-8 MONITOR?

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 MONITOR?

The FDA product code for VITALOG PMS-8 MONITOR is DQK.

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-3000K871813VITALOG PMS-8 (MODIFICATION)K845051VITALOG PMS-8

Related Devices (Code: DQK)

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.

K261729EnSite™ X EP SystemAbbott MedicalK262005Affera Integrated Mapping SystemMedtronic, Inc.K253692AVVIGO™+ Multi-Modality Guidance SystemBoston ScientificK253576CorVista System® with PCWP Add-OnAnalytics For Life, Inc.K262006EnSite™ X EP SystemAbbott MedicalK252978ScioCardio ECG Analysis PlatformSynergen Technology Labs, LLC

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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