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FDA 510(k)

MODEL #250 DEFIB CABLE

K-Number: K904466 · 1991-01-30

ApplicantCardiotronics, Inc.
Decision Date1991-01-30
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL #250 DEFIB CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Cardiotronics, Inc.. It received FDA 510(k) clearance on 1991-01-30 under 510(k) number K904466. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL #250 DEFIB CABLE?

MODEL #250 DEFIB CABLE is a medical device that received FDA 510(k) clearance on 1991-01-30. The listed applicant is Cardiotronics, Inc.. The 510(k) number is K904466.

When did MODEL #250 DEFIB CABLE receive FDA 510(k) clearance?

MODEL #250 DEFIB CABLE received FDA 510(k) clearance on 1991-01-30, under 510(k) number K904466.

Who is the listed applicant for MODEL #250 DEFIB CABLE?

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

What is the FDA product code for MODEL #250 DEFIB CABLE?

The FDA product code for MODEL #250 DEFIB CABLE is LDD.

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Other records listing Cardiotronics, 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.

K932903EKG VESTK922064MODEL #510 STEALTH-PLATE DISPERSIVE ELECTRODEK923297MODEL #340 STEALTH-TRODE+LSK922227MODEL #225-ST SHOCK-TRODE ADULT DEFIB PADS STERILEK922172MODEL # 230 ST STEALTH-TRODE DEFIB PADS (STERILE)K922173MODEL # 830 ST ADULT STIMULATION PADS (STERILE)

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Related Devices (Code: LDD)

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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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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