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FDA 510(k)

DAIG PACEMAKER LEAD ADAPTOR

K-Number: K870562 · 1987-03-03

ApplicantDaig Corp.
Decision Date1987-03-03
Product CodeDTD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DAIG PACEMAKER LEAD ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Daig Corp.. It received FDA 510(k) clearance on 1987-03-03 under 510(k) number K870562. 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 DAIG PACEMAKER LEAD ADAPTOR?

DAIG PACEMAKER LEAD ADAPTOR is a medical device that received FDA 510(k) clearance on 1987-03-03. The listed applicant is Daig Corp.. The 510(k) number is K870562.

When did DAIG PACEMAKER LEAD ADAPTOR receive FDA 510(k) clearance?

DAIG PACEMAKER LEAD ADAPTOR received FDA 510(k) clearance on 1987-03-03, under 510(k) number K870562.

Who is the listed applicant for DAIG PACEMAKER LEAD ADAPTOR?

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

What is the FDA product code for DAIG PACEMAKER LEAD ADAPTOR?

The FDA product code for DAIG PACEMAKER LEAD ADAPTOR is DTD.

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Other records listing Daig Corp. 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.

K000004ALLIANCE LEFT HEART DELIVERY SYSTEM INTRODUCER, MODEL #407509K994334ULTRA-FLEX HEMOSTASIS INTRODUCER. MODEL 406XXXK982299SPYGLASS 5 FR ANGIOGRAPHIC CATHETERK982187FAST-CATH INTRA-CARDIAC INTRODUCERK973840FAST-CATH (TM) INTRA-CARDIAC INTRODUCERK964518FAST-CATH TRANSSEPTAL CATHETER INTRODUCER

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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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