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FDA 510(k)

ASEPTICO ENDOPEX V, MODEL AEU-40

K-Number: K030895 · 2003-12-03

ApplicantAseptico, Inc.
Decision Date2003-12-03
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

ASEPTICO ENDOPEX V, MODEL AEU-40 is the device name listed in this FDA 510(k) record. The listed applicant is Aseptico, Inc.. It received FDA 510(k) clearance on 2003-12-03 under 510(k) number K030895. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASEPTICO ENDOPEX V, MODEL AEU-40?

ASEPTICO ENDOPEX V, MODEL AEU-40 is a medical device that received FDA 510(k) clearance on 2003-12-03. The listed applicant is Aseptico, Inc.. The 510(k) number is K030895.

When did ASEPTICO ENDOPEX V, MODEL AEU-40 receive FDA 510(k) clearance?

ASEPTICO ENDOPEX V, MODEL AEU-40 received FDA 510(k) clearance on 2003-12-03, under 510(k) number K030895.

Who is the listed applicant for ASEPTICO ENDOPEX V, MODEL AEU-40?

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 ENDOPEX V, MODEL AEU-40?

The FDA product code for ASEPTICO ENDOPEX V, MODEL AEU-40 is LQY.

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Related Devices (Code: LQY)

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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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