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FDA 510(k)

CLASSIC ECG/STIMULATING NO. 1700 SERIES

K-Number: K900519 · 1990-03-19

ApplicantClassic Medical Products, Inc.
Decision Date1990-03-19
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CLASSIC ECG/STIMULATING NO. 1700 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Classic Medical Products, Inc.. It received FDA 510(k) clearance on 1990-03-19 under 510(k) number K900519. 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 CLASSIC ECG/STIMULATING NO. 1700 SERIES?

CLASSIC ECG/STIMULATING NO. 1700 SERIES is a medical device that received FDA 510(k) clearance on 1990-03-19. The listed applicant is Classic Medical Products, Inc.. The 510(k) number is K900519.

When did CLASSIC ECG/STIMULATING NO. 1700 SERIES receive FDA 510(k) clearance?

CLASSIC ECG/STIMULATING NO. 1700 SERIES received FDA 510(k) clearance on 1990-03-19, under 510(k) number K900519.

Who is the listed applicant for CLASSIC ECG/STIMULATING NO. 1700 SERIES?

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

What is the FDA product code for CLASSIC ECG/STIMULATING NO. 1700 SERIES?

The FDA product code for CLASSIC ECG/STIMULATING NO. 1700 SERIES is DRX.

Related Clinical Trials

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Other records listing Classic 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.

K862953CLASSIC RESTING SILVER-SILVERCHLORIDE ELECTRODE

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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