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FDA 510(k)

COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL

K-Number: K972449 · 1997-08-20

Decision Date1997-08-20
Product CodeJSL
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL is the device name listed in this FDA 510(k) record. The listed applicant is Copan Italia Spa. It received FDA 510(k) clearance on 1997-08-20 under 510(k) number K972449. The device is classified under product code JSL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL?

COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL is a medical device that received FDA 510(k) clearance on 1997-08-20. The listed applicant is Copan Italia Spa. The 510(k) number is K972449.

When did COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL receive FDA 510(k) clearance?

COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL received FDA 510(k) clearance on 1997-08-20, under 510(k) number K972449.

Who is the listed applicant for COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL?

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

What is the FDA product code for COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL?

The FDA product code for COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL is JSL.

Related Clinical Trials

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.

Other records listing Copan Italia Spa 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.

View all 7 devices →

Related Devices (Code: JSL)

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.

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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