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FDA 510(k)

NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR

K-Number: K875199 · 1988-02-18

ApplicantBiotronik Sales, Inc.
Decision Date1988-02-18
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik Sales, Inc.. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K875199. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR?

NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Biotronik Sales, Inc.. The 510(k) number is K875199.

When did NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR receive FDA 510(k) clearance?

NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR received FDA 510(k) clearance on 1988-02-18, under 510(k) number K875199.

Who is the listed applicant for NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR?

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

What is the FDA product code for NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR?

The FDA product code for NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR is DTB.

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Other records listing Biotronik Sales, 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.

K853194ERA-20K860036EDP-20 PACEMAKERK863878TRIOS-M VS-1 PULSE GENERATORK863879NEOS-M VS-1 PULSE GENERATORK863480BIOTRONIK PERMANENT PACEMAKER ELECTRODEK860921NEOS VS-1, PULSE GENERATOR

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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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