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FDA 510(k)

VICKERS MEDICAL MODEL 271 HEART RATE MONITOR

K-Number: K854597 · 1986-05-09

ApplicantVickers , Ltd.
Decision Date1986-05-09
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VICKERS MEDICAL MODEL 271 HEART RATE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Vickers , Ltd.. It received FDA 510(k) clearance on 1986-05-09 under 510(k) number K854597. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VICKERS MEDICAL MODEL 271 HEART RATE MONITOR?

VICKERS MEDICAL MODEL 271 HEART RATE MONITOR is a medical device that received FDA 510(k) clearance on 1986-05-09. The listed applicant is Vickers , Ltd.. The 510(k) number is K854597.

When did VICKERS MEDICAL MODEL 271 HEART RATE MONITOR receive FDA 510(k) clearance?

VICKERS MEDICAL MODEL 271 HEART RATE MONITOR received FDA 510(k) clearance on 1986-05-09, under 510(k) number K854597.

Who is the listed applicant for VICKERS MEDICAL MODEL 271 HEART RATE MONITOR?

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

What is the FDA product code for VICKERS MEDICAL MODEL 271 HEART RATE MONITOR?

The FDA product code for VICKERS MEDICAL MODEL 271 HEART RATE MONITOR is DRT.

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 Vickers , Ltd. 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.

K870330SP55 SYRINGE PUMPK870279VP2000 INFUSION PUMPK854598VICKERS MEDICAL MODEL 272 TEMPERATURE MONITORK854599VICKERS MEDICAL MODEL 273 OXYGEN MONITOR

Related Devices (Code: DRT)

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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

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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