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FDA 510(k)

MODEL 5000 AMBULATORY MONITORING SYSTEM

K-Number: K871500 · 1987-07-01

ApplicantOxford Medilog, Inc.
Decision Date1987-07-01
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL 5000 AMBULATORY MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Medilog, Inc.. It received FDA 510(k) clearance on 1987-07-01 under 510(k) number K871500. 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 MODEL 5000 AMBULATORY MONITORING SYSTEM?

MODEL 5000 AMBULATORY MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1987-07-01. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K871500.

When did MODEL 5000 AMBULATORY MONITORING SYSTEM receive FDA 510(k) clearance?

MODEL 5000 AMBULATORY MONITORING SYSTEM received FDA 510(k) clearance on 1987-07-01, under 510(k) number K871500.

Who is the listed applicant for MODEL 5000 AMBULATORY MONITORING SYSTEM?

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

What is the FDA product code for MODEL 5000 AMBULATORY MONITORING SYSTEM?

The FDA product code for MODEL 5000 AMBULATORY MONITORING SYSTEM is GWQ.

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Related Devices (Code: GWQ)

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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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