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FDA 510(k)

ELECTRODE, MODEL 030-324

K-Number: K781822 · 1979-02-08

ApplicantTelectronics, Inc.
Decision Date1979-02-08
Product CodeDTD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRODE, MODEL 030-324 is the device name listed in this FDA 510(k) record. The listed applicant is Telectronics, Inc.. It received FDA 510(k) clearance on 1979-02-08 under 510(k) number K781822. The device is classified under product code DTD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRODE, MODEL 030-324?

ELECTRODE, MODEL 030-324 is a medical device that received FDA 510(k) clearance on 1979-02-08. The listed applicant is Telectronics, Inc.. The 510(k) number is K781822.

When did ELECTRODE, MODEL 030-324 receive FDA 510(k) clearance?

ELECTRODE, MODEL 030-324 received FDA 510(k) clearance on 1979-02-08, under 510(k) number K781822.

Who is the listed applicant for ELECTRODE, MODEL 030-324?

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

What is the FDA product code for ELECTRODE, MODEL 030-324?

The FDA product code for ELECTRODE, MODEL 030-324 is DTD.

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Other records listing Telectronics, Inc. as applicant

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Related Devices (Code: DTD)

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.

K1320086981M LEAD EXTENDER KIT, 6984M LEAD EXTENDER KIT, 6986M LEAD EXTENDER KIT, 5866-24M LEAD ADAPTOR KIT, 5866-38M LEAD ADAPMedtronic, Inc.K041574CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020Guidant CorporationK031164PACING LEAD ADAPTORS, BIPOLAR, MODELS ILINK-BIS, ILINK-BLVOscor, Inc.K024156PACING LEAD EXTENSIONS, BIPOLAR, PACING LEAD ADAPTORS, UNIPOLAR/BIPOLAR,PACING LEAD ADAPTORS, UNIPOLAR/BIPOLAROscor, Inc.K010787PACING LEAD BIPOLAR ADAPTERS AND EXTENSIONSOscor, Inc.K003454A1-CS-SB Y-ADAPTER, MODEL 124 871Biotronik, 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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