FDA 510(k)

MODEL 5866-26 LEAD ADAPTER KIT

K-Number: K820935 · 1982-04-16

Decision Date1982-04-16

Product CodeDTD

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MODEL 5866-26 LEAD ADAPTER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1982-04-16 under 510(k) number K820935. 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 MODEL 5866-26 LEAD ADAPTER KIT?

MODEL 5866-26 LEAD ADAPTER KIT is a medical device that received FDA 510(k) clearance on 1982-04-16. The listed applicant is Medtronic Vascular. The 510(k) number is K820935.

When did MODEL 5866-26 LEAD ADAPTER KIT receive FDA 510(k) clearance?

MODEL 5866-26 LEAD ADAPTER KIT received FDA 510(k) clearance on 1982-04-16, under 510(k) number K820935.

Who is the listed applicant for MODEL 5866-26 LEAD ADAPTER KIT?

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

What is the FDA product code for MODEL 5866-26 LEAD ADAPTER KIT?

The FDA product code for MODEL 5866-26 LEAD ADAPTER KIT is DTD.

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Related Devices (Code: DTD)

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 Corporation K031164PACING 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.