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FDA 510(k)

STOCKERT CARDIAC PACING ELECTRODES

K-Number: K812049 · 1982-03-18

ApplicantStoeckert Instrumente
Decision Date1982-03-18
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOCKERT CARDIAC PACING ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Stoeckert Instrumente. It received FDA 510(k) clearance on 1982-03-18 under 510(k) number K812049. 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 STOCKERT CARDIAC PACING ELECTRODES?

STOCKERT CARDIAC PACING ELECTRODES is a medical device that received FDA 510(k) clearance on 1982-03-18. The listed applicant is Stoeckert Instrumente. The 510(k) number is K812049.

When did STOCKERT CARDIAC PACING ELECTRODES receive FDA 510(k) clearance?

STOCKERT CARDIAC PACING ELECTRODES received FDA 510(k) clearance on 1982-03-18, under 510(k) number K812049.

Who is the listed applicant for STOCKERT CARDIAC PACING ELECTRODES?

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

What is the FDA product code for STOCKERT CARDIAC PACING ELECTRODES?

The FDA product code for STOCKERT CARDIAC PACING ELECTRODES is DTB.

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Other records listing Stoeckert Instrumente 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.

K002273STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAEK001961STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAEK002118STOCKERT COMPACT SYSTEM VERSION 2.0K992635INTERFACE MODULE IDDDK990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSK982014STOCKERT COMPACT SYSTEM

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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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