PROVOX VEGA PUNCTURE SET
K-Number: K131947 · 2013-10-18
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Device Summary
Frequently Asked Questions
What is the PROVOX VEGA PUNCTURE SET?
PROVOX VEGA PUNCTURE SET is a medical device that received FDA 510(k) clearance on 2013-10-18. The listed applicant is Atos Medical AB. The 510(k) number is K131947.
When did PROVOX VEGA PUNCTURE SET receive FDA 510(k) clearance?
PROVOX VEGA PUNCTURE SET received FDA 510(k) clearance on 2013-10-18, under 510(k) number K131947.
Who is the listed applicant for PROVOX VEGA PUNCTURE SET?
The FDA 510(k) record lists Atos Medical AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROVOX VEGA PUNCTURE SET?
The FDA product code for PROVOX VEGA PUNCTURE SET is EWL.
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 Atos Medical AB 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: EWL)
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
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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