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FDA 510(k)

SURELOCK(TM) SNAPLESS MONITORING ELECTRODE

K-Number: K931903 · 1993-10-07

ApplicantLudlow Technical Products
Decision Date1993-10-07
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SURELOCK(TM) SNAPLESS MONITORING ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Ludlow Technical Products. It received FDA 510(k) clearance on 1993-10-07 under 510(k) number K931903. 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 SURELOCK(TM) SNAPLESS MONITORING ELECTRODE?

SURELOCK(TM) SNAPLESS MONITORING ELECTRODE is a medical device that received FDA 510(k) clearance on 1993-10-07. The listed applicant is Ludlow Technical Products. The 510(k) number is K931903.

When did SURELOCK(TM) SNAPLESS MONITORING ELECTRODE receive FDA 510(k) clearance?

SURELOCK(TM) SNAPLESS MONITORING ELECTRODE received FDA 510(k) clearance on 1993-10-07, under 510(k) number K931903.

Who is the listed applicant for SURELOCK(TM) SNAPLESS MONITORING ELECTRODE?

The FDA 510(k) record lists Ludlow Technical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURELOCK(TM) SNAPLESS MONITORING ELECTRODE?

The FDA product code for SURELOCK(TM) SNAPLESS MONITORING ELECTRODE is DRX.

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Other records listing Ludlow Technical Products 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.

K991235SOFTRANS TEMP INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 5000, SOFTRANS TEMP IUPC)K973110LUDLOW TECHNICAL PRODUCTS, ELECTRODE, ELECTROSURGICAL, DISPOSABLE PEDIATRIC DISPERSIVE ELECTRODES; WITH AND WITHOUT CORDK972646AD-HEAL HYDROGEL DRESSING, VARIOUS SIZESK964401KENDALL-LTP DISPOSABLE TEMPERATURE PROBES (DTP1,DTP2,DTP3,DTP4)

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

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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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