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FDA 510(k)

NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT

K-Number: K033328 · 2004-01-16

ApplicantNovosci Corp.
Decision Date2004-01-16
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT is the device name listed in this FDA 510(k) record. The listed applicant is Novosci Corp.. It received FDA 510(k) clearance on 2004-01-16 under 510(k) number K033328. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT?

NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT is a medical device that received FDA 510(k) clearance on 2004-01-16. The listed applicant is Novosci Corp.. The 510(k) number is K033328.

When did NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT receive FDA 510(k) clearance?

NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT received FDA 510(k) clearance on 2004-01-16, under 510(k) number K033328.

Who is the listed applicant for NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT?

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

What is the FDA product code for NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT?

The FDA product code for NOVOSCI TUBING AND CONNECTORS WITH NOVOCOAT TREATMENT is DTL.

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Other records listing Novosci Corp. 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.

K063355D-LINE CATHETER ST, DOUBLE LUMEN ST; EXTRA FLOWK033270NOVOSCI READY SYSTEM, MODEL RS-200

Related Devices (Code: DTL)

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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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