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FDA 510(k)

AN3100 MULHOLLAND DRAIN

K-Number: K872459 · 1987-07-21

Decision Date1987-07-21
Product CodeGBS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AN3100 MULHOLLAND DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is H.W. Andersen Products, Inc.. It received FDA 510(k) clearance on 1987-07-21 under 510(k) number K872459. The device is classified under product code GBS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AN3100 MULHOLLAND DRAIN?

AN3100 MULHOLLAND DRAIN is a medical device that received FDA 510(k) clearance on 1987-07-21. The listed applicant is H.W. Andersen Products, Inc.. The 510(k) number is K872459.

When did AN3100 MULHOLLAND DRAIN receive FDA 510(k) clearance?

AN3100 MULHOLLAND DRAIN received FDA 510(k) clearance on 1987-07-21, under 510(k) number K872459.

Who is the listed applicant for AN3100 MULHOLLAND DRAIN?

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

What is the FDA product code for AN3100 MULHOLLAND DRAIN?

The FDA product code for AN3100 MULHOLLAND DRAIN is GBS.

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 H.W. Andersen Products, 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.

Related Devices (Code: GBS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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