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FDA 510(k)

ACTIVE ADAPTER

K-Number: K904506 · 1990-12-13

ApplicantBeacon Laboratories, Inc.
Decision Date1990-12-13
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACTIVE ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Beacon Laboratories, Inc.. It received FDA 510(k) clearance on 1990-12-13 under 510(k) number K904506. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTIVE ADAPTER?

ACTIVE ADAPTER is a medical device that received FDA 510(k) clearance on 1990-12-13. The listed applicant is Beacon Laboratories, Inc.. The 510(k) number is K904506.

When did ACTIVE ADAPTER receive FDA 510(k) clearance?

ACTIVE ADAPTER received FDA 510(k) clearance on 1990-12-13, under 510(k) number K904506.

Who is the listed applicant for ACTIVE ADAPTER?

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

What is the FDA product code for ACTIVE ADAPTER?

The FDA product code for ACTIVE ADAPTER is GEI.

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Other records listing Beacon Laboratories, Inc. as applicant

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Related Devices (Code: GEI)

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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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