Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016489995

FEI Number

3016489995

Entity Name

OXAVITA S.R.L.

City/State/Country

Buenos Aires, AR

Establishment Address

Ceretti 3320 CABA, Buenos Aires 1431, AR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Oxavita S.R.L. (Owner Number: 10062498)

Owner / Operator Contact Address

Ceretti 3320 CABA, Buenos Aires, AR-B 1431, AR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K171899

PMA Number

N/A

All Registered Proprietary Names

Revitalair 430F

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CBF	Chamber, Hyperbaric	Anesthesiology	Class 2	868.5470	2020-02-03

Official Correspondent

Jorge Millan

US Agent Details

Jorge Millan Business: Sigma Scientific Services Email: jmillan@sigmabiomedical.com Phone: (786) 4165587

Related Public Records

Same Entity

Oxavita S.R.L.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016489995. Last updated year: 2026. Please use registration number 3016489995 when referencing this establishment in official correspondence.