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FDA 510(k)

ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925

K-Number: K030163 · 2003-03-03

Decision Date2003-03-03
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925 is the device name listed in this FDA 510(k) record. The listed applicant is Aseptico, Inc.. It received FDA 510(k) clearance on 2003-03-03 under 510(k) number K030163. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925?

ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925 is a medical device that received FDA 510(k) clearance on 2003-03-03. The listed applicant is Aseptico, Inc.. The 510(k) number is K030163.

When did ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925 receive FDA 510(k) clearance?

ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925 received FDA 510(k) clearance on 2003-03-03, under 510(k) number K030163.

Who is the listed applicant for ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925?

The FDA 510(k) record lists Aseptico, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925?

The FDA product code for ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925 is EKX.

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 Aseptico, Inc. 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.

View all 16 devices →

Related Devices (Code: EKX)

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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