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FDA 510(k)

MEDILOG STRESSLINK

K-Number: K951128 · 1996-08-28

ApplicantOxford Medical, Inc.
Decision Date1996-08-28
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDILOG STRESSLINK is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Medical, Inc.. It received FDA 510(k) clearance on 1996-08-28 under 510(k) number K951128. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILOG STRESSLINK?

MEDILOG STRESSLINK is a medical device that received FDA 510(k) clearance on 1996-08-28. The listed applicant is Oxford Medical, Inc.. The 510(k) number is K951128.

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

MEDILOG STRESSLINK received FDA 510(k) clearance on 1996-08-28, under 510(k) number K951128.

Who is the listed applicant for MEDILOG STRESSLINK?

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

What is the FDA product code for MEDILOG STRESSLINK?

The FDA product code for MEDILOG STRESSLINK is DPS.

Related Clinical Trials

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Other records listing Oxford Medical, Inc. 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.

K885256MEDILOG EXCEL ECG ANALYSIS SYSTEM

Related Devices (Code: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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