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FDA 510(k)

MODEL RZ PACEMAKER LEAD VARIOUS

K-Number: K823894 · 1983-04-30

ApplicantDr. Ing. P. Osypka, GmbH
Decision Date1983-04-30
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL RZ PACEMAKER LEAD VARIOUS is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Ing. P. Osypka, GmbH. It received FDA 510(k) clearance on 1983-04-30 under 510(k) number K823894. 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 MODEL RZ PACEMAKER LEAD VARIOUS?

MODEL RZ PACEMAKER LEAD VARIOUS is a medical device that received FDA 510(k) clearance on 1983-04-30. The listed applicant is Dr. Ing. P. Osypka, GmbH. The 510(k) number is K823894.

When did MODEL RZ PACEMAKER LEAD VARIOUS receive FDA 510(k) clearance?

MODEL RZ PACEMAKER LEAD VARIOUS received FDA 510(k) clearance on 1983-04-30, under 510(k) number K823894.

Who is the listed applicant for MODEL RZ PACEMAKER LEAD VARIOUS?

The FDA 510(k) record lists Dr. Ing. P. Osypka, GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL RZ PACEMAKER LEAD VARIOUS?

The FDA product code for MODEL RZ PACEMAKER LEAD VARIOUS 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 Dr. Ing. P. Osypka, GmbH 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.

K823892MODEL SZ PACEMAKER LEAD-VARIOUSK823896MODEL FF..D & FX..D PACEMAKER LEADS

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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