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FDA 510(k)

ALBG

K-Number: K981468 · 1998-05-27

ApplicantAbbott Laboratories
Decision Date1998-05-27
Product CodeCIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ALBG is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1998-05-27 under 510(k) number K981468. The device is classified under product code CIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALBG?

ALBG is a medical device that received FDA 510(k) clearance on 1998-05-27. The listed applicant is Abbott Laboratories. The 510(k) number is K981468.

When did ALBG receive FDA 510(k) clearance?

ALBG received FDA 510(k) clearance on 1998-05-27, under 510(k) number K981468.

Who is the listed applicant for ALBG?

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

What is the FDA product code for ALBG?

The FDA product code for ALBG is CIX.

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Related Devices (Code: CIX)

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.

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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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