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FDA 510(k)

MODIFICATION OF NOGA

K-Number: K990494 · 1999-09-03

ApplicantBiosense, Inc.
Decision Date1999-09-03
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF NOGA is the device name listed in this FDA 510(k) record. The listed applicant is Biosense, Inc.. It received FDA 510(k) clearance on 1999-09-03 under 510(k) number K990494. 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 OF NOGA?

MODIFICATION OF NOGA is a medical device that received FDA 510(k) clearance on 1999-09-03. The listed applicant is Biosense, Inc.. The 510(k) number is K990494.

When did MODIFICATION OF NOGA receive FDA 510(k) clearance?

MODIFICATION OF NOGA received FDA 510(k) clearance on 1999-09-03, under 510(k) number K990494.

Who is the listed applicant for MODIFICATION OF NOGA?

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

What is the FDA product code for MODIFICATION OF NOGA?

The FDA product code for MODIFICATION OF NOGA is DQK.

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Related Devices (Code: DQK)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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