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FDA 510(k)

COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGE

K-Number: K964060 · 1996-12-24

Decision Date1996-12-24
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGE is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories (Israel) , Ltd.. It received FDA 510(k) clearance on 1996-12-24 under 510(k) number K964060. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGE?

COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGE is a medical device that received FDA 510(k) clearance on 1996-12-24. The listed applicant is Travenol Laboratories (Israel) , Ltd.. The 510(k) number is K964060.

When did COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGE receive FDA 510(k) clearance?

COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGE received FDA 510(k) clearance on 1996-12-24, under 510(k) number K964060.

Who is the listed applicant for COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGE?

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

What is the FDA product code for COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGE?

The FDA product code for COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGE is FMF.

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.

Related Devices (Code: FMF)

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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