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FDA 510(k)

MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE

K-Number: K990266 · 1999-02-02

ApplicantMicromedical Industries, Ltd.
Decision Date1999-02-02
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Micromedical Industries, Ltd.. It received FDA 510(k) clearance on 1999-02-02 under 510(k) number K990266. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE?

MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE is a medical device that received FDA 510(k) clearance on 1999-02-02. The listed applicant is Micromedical Industries, Ltd.. The 510(k) number is K990266.

When did MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE receive FDA 510(k) clearance?

MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE received FDA 510(k) clearance on 1999-02-02, under 510(k) number K990266.

Who is the listed applicant for MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE?

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

What is the FDA product code for MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE?

The FDA product code for MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE is LOS.

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 Micromedical Industries, Ltd. 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.

K013311MODIFICATION TO: POCKETVIEW ECG SOFTWAREK012540BLY-501 ADAPTORK922528CMS SYSTEMK915624MODIFIED BIOLOGK915627PACEVIEW

Related Devices (Code: LOS)

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.

K090895EKG-PLUS II SOFTWAREBionet Co., Ltd.K083749CARDIOVIEW32 REVIEW MODULEQrs Diagnostic, LLCK073376PHILIPS ECG ALGORITHMPhilips Medical SystemsK023034CARDIOTOUCH-3000Bionet Company, Ltd.K011328CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPHBionet Company, Ltd.K993616CARDIO-CARD INTERPRETATION SYSTEM INasiff Assoc., Inc.

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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