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FDA 510(k)

VITALOG PMS-8

K-Number: K845051 · 1985-05-15

ApplicantVitalog Corp.
Decision Date1985-05-15
Product CodeDPZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITALOG PMS-8 is the device name listed in this FDA 510(k) record. The listed applicant is Vitalog Corp.. It received FDA 510(k) clearance on 1985-05-15 under 510(k) number K845051. The device is classified under product code DPZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALOG PMS-8?

VITALOG PMS-8 is a medical device that received FDA 510(k) clearance on 1985-05-15. The listed applicant is Vitalog Corp.. The 510(k) number is K845051.

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

VITALOG PMS-8 received FDA 510(k) clearance on 1985-05-15, under 510(k) number K845051.

Who is the listed applicant for VITALOG PMS-8?

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?

The FDA product code for VITALOG PMS-8 is DPZ.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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)K812739VITALOG PMS-8 MONITOR

Related Devices (Code: DPZ)

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.

K042675FLEXI-STAT SP02 EAR SENSORElekon Industries U.S.A., Inc.K040831DATEX-OHMEDA TRUSAT PULSE OXIMETER AND ACCESSORIES, MODEL 3500Datex-Ohmeda, Inc.K012333FLEXI-SITE SP02 EAR SENSOREpic Medical Equipment Services, Inc.K010718FLEXI-SITE SP02 EAR SENSOREpic Medical Equipment Services, Inc.K944760DURA-Y OXYGEN TRANSDUCER, EAR CLIPNellcor, Inc.K942752MARQUETTE EAR PROBE SENSORMarquette Electronics, 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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