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FDA 510(k)

MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR

K-Number: K896103 · 1990-01-18

ApplicantAdvanced Medical Products, Inc.
Decision Date1990-01-18
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Products, Inc.. It received FDA 510(k) clearance on 1990-01-18 under 510(k) number K896103. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR?

MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR is a medical device that received FDA 510(k) clearance on 1990-01-18. The listed applicant is Advanced Medical Products, Inc.. The 510(k) number is K896103.

When did MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR receive FDA 510(k) clearance?

MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR received FDA 510(k) clearance on 1990-01-18, under 510(k) number K896103.

Who is the listed applicant for MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR?

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

What is the FDA product code for MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR?

The FDA product code for MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR is DSI.

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Other records listing Advanced Medical Products, 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.

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Related Devices (Code: DSI)

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.

K243349BodyGuardian Remote Monitoring System (BGRMS v3.0)Boston Scientific Cardiac Diagnostic Technologies, Inc.K250356MoMe ARC® Wireless Ambulatory ECG Monitoring and Detection System (32000)Infobionic, Inc.K240177Zio AT® device (A100A1001)iRhythm Technologies, Inc.K230265MoMe® ARC Wireless Ambulatory ECG Monitoring and Detection SystemInfobionic, Inc.K231276SmartCardia 7L PlatformSmartcardia SAK193104Unified Arrhythmia Diagnostic System PocketECG IVMedicalgorithmics S.A.

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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