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FDA 510(k)

VIPI BLOCK

K-Number: K102341 · 2010-12-16

ApplicantVipi Industria,Comercio,Exportacao E Importacao DE
Decision Date2010-12-16
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VIPI BLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Vipi Industria,Comercio,Exportacao E Importacao DE. It received FDA 510(k) clearance on 2010-12-16 under 510(k) number K102341. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIPI BLOCK?

VIPI BLOCK is a medical device that received FDA 510(k) clearance on 2010-12-16. The listed applicant is Vipi Industria,Comercio,Exportacao E Importacao DE. The 510(k) number is K102341.

When did VIPI BLOCK receive FDA 510(k) clearance?

VIPI BLOCK received FDA 510(k) clearance on 2010-12-16, under 510(k) number K102341.

Who is the listed applicant for VIPI BLOCK?

The FDA 510(k) record lists Vipi Industria,Comercio,Exportacao E Importacao DE as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIPI BLOCK?

The FDA product code for VIPI BLOCK is EBG.

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Related Devices (Code: EBG)

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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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