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FDA 510(k)

MICROCOR E.C.G. MONITOR WITH A.C. ADAPTER

K-Number: K861281 · 1986-08-01

ApplicantMicrocor, Inc.
Decision Date1986-08-01
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROCOR E.C.G. MONITOR WITH A.C. ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Microcor, Inc.. It received FDA 510(k) clearance on 1986-08-01 under 510(k) number K861281. 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 MICROCOR E.C.G. MONITOR WITH A.C. ADAPTER?

MICROCOR E.C.G. MONITOR WITH A.C. ADAPTER is a medical device that received FDA 510(k) clearance on 1986-08-01. The listed applicant is Microcor, Inc.. The 510(k) number is K861281.

When did MICROCOR E.C.G. MONITOR WITH A.C. ADAPTER receive FDA 510(k) clearance?

MICROCOR E.C.G. MONITOR WITH A.C. ADAPTER received FDA 510(k) clearance on 1986-08-01, under 510(k) number K861281.

Who is the listed applicant for MICROCOR E.C.G. MONITOR WITH A.C. ADAPTER?

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

What is the FDA product code for MICROCOR E.C.G. MONITOR WITH A.C. ADAPTER?

The FDA product code for MICROCOR E.C.G. MONITOR WITH A.C. ADAPTER is DPS.

Related Clinical Trials

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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Other records listing Microcor, 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.

K851325MICROCOR ECG MONITOR

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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