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FDA 510(k)

TE ME NA LOSS OF RESISTANCE SYRINGE, 10CC

K-Number: K990020 · 1999-06-24

Decision Date1999-06-24
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TE ME NA LOSS OF RESISTANCE SYRINGE, 10CC is the device name listed in this FDA 510(k) record. The listed applicant is Te ME NA S.A.R.L.. It received FDA 510(k) clearance on 1999-06-24 under 510(k) number K990020. 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 TE ME NA LOSS OF RESISTANCE SYRINGE, 10CC?

TE ME NA LOSS OF RESISTANCE SYRINGE, 10CC is a medical device that received FDA 510(k) clearance on 1999-06-24. The listed applicant is Te ME NA S.A.R.L.. The 510(k) number is K990020.

When did TE ME NA LOSS OF RESISTANCE SYRINGE, 10CC receive FDA 510(k) clearance?

TE ME NA LOSS OF RESISTANCE SYRINGE, 10CC received FDA 510(k) clearance on 1999-06-24, under 510(k) number K990020.

Who is the listed applicant for TE ME NA LOSS OF RESISTANCE SYRINGE, 10CC?

The FDA 510(k) record lists Te ME NA S.A.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TE ME NA LOSS OF RESISTANCE SYRINGE, 10CC?

The FDA product code for TE ME NA LOSS OF RESISTANCE SYRINGE, 10CC 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.

Other records listing Te ME NA S.A.R.L. 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.

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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