VERSEO AIR PRESSURE MASSAGER
K-Number: K092435 · 2010-03-09
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Device Summary
Frequently Asked Questions
What is the VERSEO AIR PRESSURE MASSAGER?
VERSEO AIR PRESSURE MASSAGER is a medical device that received FDA 510(k) clearance on 2010-03-09. The listed applicant is The American Export Group & International Services. The 510(k) number is K092435.
When did VERSEO AIR PRESSURE MASSAGER receive FDA 510(k) clearance?
VERSEO AIR PRESSURE MASSAGER received FDA 510(k) clearance on 2010-03-09, under 510(k) number K092435.
Who is the listed applicant for VERSEO AIR PRESSURE MASSAGER?
The FDA 510(k) record lists The American Export Group & International Services as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERSEO AIR PRESSURE MASSAGER?
The FDA product code for VERSEO AIR PRESSURE MASSAGER is IRP.
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: IRP)
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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