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FDA 510(k)

NOGA

K-Number: K960542 · 1996-04-15

ApplicantBiosense, Ltd.
Decision Date1996-04-15
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NOGA is the device name listed in this FDA 510(k) record. The listed applicant is Biosense, Ltd.. It received FDA 510(k) clearance on 1996-04-15 under 510(k) number K960542. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOGA?

NOGA is a medical device that received FDA 510(k) clearance on 1996-04-15. The listed applicant is Biosense, Ltd.. The 510(k) number is K960542.

When did NOGA receive FDA 510(k) clearance?

NOGA received FDA 510(k) clearance on 1996-04-15, under 510(k) number K960542.

Who is the listed applicant for NOGA?

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

What is the FDA product code for NOGA?

The FDA product code for NOGA is DRF.

Other records listing Biosense, Ltd. 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.

K961903MAGELLANK954395CARTO SYSTEM

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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.

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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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