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FDA 510(k)

ESOPHAGEAL PILL ELECTRODE

K-Number: K810895 · 1981-05-13

ApplicantCon Med Equipment, Inc.
Decision Date1981-05-13
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 Con Med Equipment, Inc.. It received FDA 510(k) clearance on 1981-05-13 under 510(k) number K810895. 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 1981-05-13. The listed applicant is Con Med Equipment, Inc.. The 510(k) number is K810895.

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

ESOPHAGEAL PILL ELECTRODE received FDA 510(k) clearance on 1981-05-13, under 510(k) number K810895.

Who is the listed applicant for ESOPHAGEAL PILL ELECTRODE?

The FDA 510(k) record lists Con Med Equipment, Inc. 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 Con Med Equipment, 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.

K830613ELECTROSURGICAL GROUND PAD-DISPERSIVEK810896VENTI-GARD JR.

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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