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FDA 510(k)

OSCOR PERMANENT PACING LEAD RZ MODEL SERIES

K-Number: K003918 · 2001-05-22

ApplicantOscor, Inc.
Decision Date2001-05-22
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

OSCOR PERMANENT PACING LEAD RZ MODEL SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Oscor, Inc.. It received FDA 510(k) clearance on 2001-05-22 under 510(k) number K003918. 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 OSCOR PERMANENT PACING LEAD RZ MODEL SERIES?

OSCOR PERMANENT PACING LEAD RZ MODEL SERIES is a medical device that received FDA 510(k) clearance on 2001-05-22. The listed applicant is Oscor, Inc.. The 510(k) number is K003918.

When did OSCOR PERMANENT PACING LEAD RZ MODEL SERIES receive FDA 510(k) clearance?

OSCOR PERMANENT PACING LEAD RZ MODEL SERIES received FDA 510(k) clearance on 2001-05-22, under 510(k) number K003918.

Who is the listed applicant for OSCOR PERMANENT PACING LEAD RZ MODEL SERIES?

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

What is the FDA product code for OSCOR PERMANENT PACING LEAD RZ MODEL SERIES?

The FDA product code for OSCOR PERMANENT PACING LEAD RZ MODEL SERIES is DTB.

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Other records listing Oscor, Inc. as applicant

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K210627Breezeway IIK130104GUIDEWIRE, PURSUER SERIESK122958DELIVERY SHEATH, MODEL ADELANTE BREEZEWAYK122960STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINOK122084INTRODUCER SET, MODEL ADELANTE-S SERIESK120459STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO

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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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