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FDA 510(k)

NOVA-PULSE

K-Number: K043302 · 2005-01-03

ApplicantNova Ranger, Inc.
Decision Date2005-01-03
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NOVA-PULSE is the device name listed in this FDA 510(k) record. The listed applicant is Nova Ranger, Inc.. It received FDA 510(k) clearance on 2005-01-03 under 510(k) number K043302. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA-PULSE?

NOVA-PULSE is a medical device that received FDA 510(k) clearance on 2005-01-03. The listed applicant is Nova Ranger, Inc.. The 510(k) number is K043302.

When did NOVA-PULSE receive FDA 510(k) clearance?

NOVA-PULSE received FDA 510(k) clearance on 2005-01-03, under 510(k) number K043302.

Who is the listed applicant for NOVA-PULSE?

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

What is the FDA product code for NOVA-PULSE?

The FDA product code for NOVA-PULSE is EBZ.

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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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