AN3100 MULHOLLAND DRAIN
K-Number: K872459 · 1987-07-21
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Device Summary
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
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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