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FDA 510(k)

ASEPTIMINI UNIT, ADU-10

K-Number: K905401 · 1991-02-20

ApplicantAseptico, Inc.
Decision Date1991-02-20
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ASEPTIMINI UNIT, ADU-10 is the device name listed in this FDA 510(k) record. The listed applicant is Aseptico, Inc.. It received FDA 510(k) clearance on 1991-02-20 under 510(k) number K905401. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASEPTIMINI UNIT, ADU-10?

ASEPTIMINI UNIT, ADU-10 is a medical device that received FDA 510(k) clearance on 1991-02-20. The listed applicant is Aseptico, Inc.. The 510(k) number is K905401.

When did ASEPTIMINI UNIT, ADU-10 receive FDA 510(k) clearance?

ASEPTIMINI UNIT, ADU-10 received FDA 510(k) clearance on 1991-02-20, under 510(k) number K905401.

Who is the listed applicant for ASEPTIMINI UNIT, ADU-10?

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 ASEPTIMINI UNIT, ADU-10?

The FDA product code for ASEPTIMINI UNIT, ADU-10 is EIA.

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Related Devices (Code: EIA)

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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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