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FDA 510(k)

TIR/TIJ AND POLYROX

K-Number: K972500 · 1998-03-04

ApplicantBiotronik, Inc.
Decision Date1998-03-04
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent - Subject to Tracking & PMS

Device Summary

TIR/TIJ AND POLYROX is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik, Inc.. It received FDA 510(k) clearance on 1998-03-04 under 510(k) number K972500. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking & PMS.

Frequently Asked Questions

What is the TIR/TIJ AND POLYROX?

TIR/TIJ AND POLYROX is a medical device that received FDA 510(k) clearance on 1998-03-04. The listed applicant is Biotronik, Inc.. The 510(k) number is K972500.

When did TIR/TIJ AND POLYROX receive FDA 510(k) clearance?

TIR/TIJ AND POLYROX received FDA 510(k) clearance on 1998-03-04, under 510(k) number K972500.

Who is the listed applicant for TIR/TIJ AND POLYROX?

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

What is the FDA product code for TIR/TIJ AND POLYROX?

The FDA product code for TIR/TIJ AND POLYROX is DTB.

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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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