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FDA 510(k)

MEDILOG FD4

K-Number: K970902 · 1997-05-05

ApplicantOxford Instruments Medical Systems
Decision Date1997-05-05
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDILOG FD4 is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Instruments Medical Systems. It received FDA 510(k) clearance on 1997-05-05 under 510(k) number K970902. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILOG FD4?

MEDILOG FD4 is a medical device that received FDA 510(k) clearance on 1997-05-05. The listed applicant is Oxford Instruments Medical Systems. The 510(k) number is K970902.

When did MEDILOG FD4 receive FDA 510(k) clearance?

MEDILOG FD4 received FDA 510(k) clearance on 1997-05-05, under 510(k) number K970902.

Who is the listed applicant for MEDILOG FD4?

The FDA 510(k) record lists Oxford Instruments Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDILOG FD4?

The FDA product code for MEDILOG FD4 is DSH.

Related Clinical Trials

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Other records listing Oxford Instruments Medical Systems 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.

K992607SONICAID SYSTEM 8002K984052SYNERGY IOM SYSTEMK961638MEDILOG MPA-SK943862SONICAID MODEL MR-63 AMBULATORY ECG RECORDER

Related Devices (Code: DSH)

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.

K260157LifeLens Physiological MonitorLifeLens Technologies, Inc.K252389Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)Smwmed, Inc.K253293VitaloJAK Clinic (Model 7100)Vitalograph , Ltd.K243650Zio® monitor (DFG0001)iRhythm Technologies, Inc.K243603AeviceMDAevice Health Pte. , Ltd.K242583AT-Patch (ATP-C130/ATP-C70)Atsens Co., Ltd.

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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