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FDA 510(k)

PACING LEADS MODEL 3262VU/VB, 3362VU/VB, 3380/3390

K-Number: K874743 · 1988-01-19

ApplicantPace Medical
Decision Date1988-01-19
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PACING LEADS MODEL 3262VU/VB, 3362VU/VB, 3380/3390 is the device name listed in this FDA 510(k) record. The listed applicant is Pace Medical. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K874743. 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 PACING LEADS MODEL 3262VU/VB, 3362VU/VB, 3380/3390?

PACING LEADS MODEL 3262VU/VB, 3362VU/VB, 3380/3390 is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Pace Medical. The 510(k) number is K874743.

When did PACING LEADS MODEL 3262VU/VB, 3362VU/VB, 3380/3390 receive FDA 510(k) clearance?

PACING LEADS MODEL 3262VU/VB, 3362VU/VB, 3380/3390 received FDA 510(k) clearance on 1988-01-19, under 510(k) number K874743.

Who is the listed applicant for PACING LEADS MODEL 3262VU/VB, 3362VU/VB, 3380/3390?

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

What is the FDA product code for PACING LEADS MODEL 3262VU/VB, 3362VU/VB, 3380/3390?

The FDA product code for PACING LEADS MODEL 3262VU/VB, 3362VU/VB, 3380/3390 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 Pace Medical 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.

K011980ADAPTER, PACING ANALYZER/UNIVERSAL PACING ADAPTER, MODELS 4820 AND 4825K012392DISPOSABLE SURGICAL EXTENSION CABLE, MODEL 4255 AND MODEL 4260K002204PACEMAKER EXTENSION CABLE MODELS 4265,4265A, 4265V, 5265, 5265A, 5265VK002496MODEL 4815 ADAPTERK002497MODEL 4810 ANALYZER OUTPUT ADAPTERK001180TEMPORARY PACEMAKER EXTENSION CABLE, MODELS 5235, 5235A, 5235V, TEMPORARY PACEMAKER SURGICAL EXTENSION CABLE, MODELS 528

View all 19 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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