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FDA 510(k)

MODIFICATION TO: ENSITE SYSTEM, MODEL, EE3000

K-Number: K070902 · 2007-05-01

ApplicantSt Jude Medical
Decision Date2007-05-01
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: ENSITE SYSTEM, MODEL, EE3000 is the device name listed in this FDA 510(k) record. The listed applicant is St Jude Medical. It received FDA 510(k) clearance on 2007-05-01 under 510(k) number K070902. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO: ENSITE SYSTEM, MODEL, EE3000?

MODIFICATION TO: ENSITE SYSTEM, MODEL, EE3000 is a medical device that received FDA 510(k) clearance on 2007-05-01. The listed applicant is St Jude Medical. The 510(k) number is K070902.

When did MODIFICATION TO: ENSITE SYSTEM, MODEL, EE3000 receive FDA 510(k) clearance?

MODIFICATION TO: ENSITE SYSTEM, MODEL, EE3000 received FDA 510(k) clearance on 2007-05-01, under 510(k) number K070902.

Who is the listed applicant for MODIFICATION TO: ENSITE SYSTEM, MODEL, EE3000?

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

What is the FDA product code for MODIFICATION TO: ENSITE SYSTEM, MODEL, EE3000?

The FDA product code for MODIFICATION TO: ENSITE SYSTEM, MODEL, EE3000 is DQK.

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Related Devices (Code: DQK)

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.

K261729EnSite™ X EP SystemAbbott MedicalK262005Affera Integrated Mapping SystemMedtronic, Inc.K253692AVVIGO™+ Multi-Modality Guidance SystemBoston ScientificK253576CorVista System® with PCWP Add-OnAnalytics For Life, Inc.K262006EnSite™ X EP SystemAbbott MedicalK252978ScioCardio ECG Analysis PlatformSynergen Technology Labs, LLC

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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