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FDA 510(k)

MODEL MICRO FD+ AMBULATORY ECG MONITOR

K-Number: K872508 · 1987-09-25

ApplicantAdvanced Medical Products, Inc.
Decision Date1987-09-25
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL MICRO FD+ AMBULATORY ECG 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 1987-09-25 under 510(k) number K872508. 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 MODEL MICRO FD+ AMBULATORY ECG MONITOR?

MODEL MICRO FD+ AMBULATORY ECG MONITOR is a medical device that received FDA 510(k) clearance on 1987-09-25. The listed applicant is Advanced Medical Products, Inc.. The 510(k) number is K872508.

When did MODEL MICRO FD+ AMBULATORY ECG MONITOR receive FDA 510(k) clearance?

MODEL MICRO FD+ AMBULATORY ECG MONITOR received FDA 510(k) clearance on 1987-09-25, under 510(k) number K872508.

Who is the listed applicant for MODEL MICRO FD+ AMBULATORY ECG 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 MODEL MICRO FD+ AMBULATORY ECG MONITOR?

The FDA product code for MODEL MICRO FD+ AMBULATORY ECG MONITOR is DSH.

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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.

K000932ARACHNOPHLEBECTOMY NEEDLEK923995URODYNAMICS TUBING KITS #5161, #5150, #7170K921426ULTRA PCIK912925ULTRA PVDK915658SPECTRA ECGK896102MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR

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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

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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