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FDA 510(k)

CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD

K-Number: K955550 · 1996-06-19

ApplicantIntermedics, Inc.
Decision Date1996-06-19
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics, Inc.. It received FDA 510(k) clearance on 1996-06-19 under 510(k) number K955550. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD?

CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD is a medical device that received FDA 510(k) clearance on 1996-06-19. The listed applicant is Intermedics, Inc.. The 510(k) number is K955550.

When did CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD receive FDA 510(k) clearance?

CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD received FDA 510(k) clearance on 1996-06-19, under 510(k) number K955550.

Who is the listed applicant for CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD?

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

What is the FDA product code for CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD?

The FDA product code for CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD is DTB.

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 Intermedics, 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.

K954610MODEL 430-07 ENDOCARDIAL PACING LEADK955122INTERMEDICS MODEL 436-07 BIPOLAR & MODEL 437-07 UNIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEADK962174BIPLR IM EN PAC LEADS (430-07,432-03,436-02 & 07, 438-05 & 07)K960281IMPLANTABLE PACING LEADS/IMPLANTABLE ACCESSORY/NON-IMPLANTABLE ACCESSORYK954719INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEADK933278INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04

View all 211 devices →

Related Devices (Code: DTB)

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.

K061212BIOTRONIK ENDOCARDIAL PACING LEADSBiotronik, Inc.K041809PERMANENT PACING LEAD, MODEL PY2Oscor, Inc.K040569PERMANENT PACING LEAD, MODEL REFINO, MODEL: REFINO-R, RU, RJUOscor, Inc.K031274MODEL 5071 MYOCARDIAL PACING LEADMedtronic VascularK031210MODEL 4951M MYOCARDIAL UNIPOLAR LEADMetronic, Inc.K023205ELOX P 45-BP; ELOX P 53-BP; ELOX P 60-BPBiotronik, 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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