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FDA 510(k)

NOVOFLO CATHETER LT

K-Number: K072499 · 2007-10-30

ApplicantNovosci, Inc.
Decision Date2007-10-30
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

NOVOFLO CATHETER LT is the device name listed in this FDA 510(k) record. The listed applicant is Novosci, Inc.. It received FDA 510(k) clearance on 2007-10-30 under 510(k) number K072499. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NOVOFLO CATHETER LT?

NOVOFLO CATHETER LT is a medical device that received FDA 510(k) clearance on 2007-10-30. The listed applicant is Novosci, Inc.. The 510(k) number is K072499.

When did NOVOFLO CATHETER LT receive FDA 510(k) clearance?

NOVOFLO CATHETER LT received FDA 510(k) clearance on 2007-10-30, under 510(k) number K072499.

Who is the listed applicant for NOVOFLO CATHETER LT?

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

What is the FDA product code for NOVOFLO CATHETER LT?

The FDA product code for NOVOFLO CATHETER LT is MSD.

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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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