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FDA 510(k)

ESOPHAGEAL PILL-ELECTRODE

K-Number: K800201 · 1980-02-26

ApplicantArzbaecher & Co.
Decision Date1980-02-26
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ESOPHAGEAL PILL-ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Arzbaecher & Co.. It received FDA 510(k) clearance on 1980-02-26 under 510(k) number K800201. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESOPHAGEAL PILL-ELECTRODE?

ESOPHAGEAL PILL-ELECTRODE is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Arzbaecher & Co.. The 510(k) number is K800201.

When did ESOPHAGEAL PILL-ELECTRODE receive FDA 510(k) clearance?

ESOPHAGEAL PILL-ELECTRODE received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800201.

Who is the listed applicant for ESOPHAGEAL PILL-ELECTRODE?

The FDA 510(k) record lists Arzbaecher & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESOPHAGEAL PILL-ELECTRODE?

The FDA product code for ESOPHAGEAL PILL-ELECTRODE is DRX.

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 Arzbaecher & Co. 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.

K792283ESOPHAGEAL ECG PREAMPLIFIER & SIGNAL CON

Related Devices (Code: DRX)

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.

K171244PhysiotraceNimbleheart, Inc.K123658BIOMODULE 3-M1Zephyr Technology CorporationK101576CENTERRIDGE DIAGNOSTIC ECG ELECTRODE, CENTERRIDGE MONITORING ECG ELECTRODESTeam Innovations, Inc.K101685IP-SETIntegral Process SasK100129AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO XAmbu A/SK093327INTCO TAB ELECTRODEShanghai Intco Electrode Manufacturing 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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