MAXI SHIELDS
K-Number: K831593 · 1983-08-12
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Device Summary
Frequently Asked Questions
What is the MAXI SHIELDS?
MAXI SHIELDS is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Weyerhaeuser Co.. The 510(k) number is K831593.
When did MAXI SHIELDS receive FDA 510(k) clearance?
MAXI SHIELDS received FDA 510(k) clearance on 1983-08-12, under 510(k) number K831593.
Who is the listed applicant for MAXI SHIELDS?
The FDA 510(k) record lists Weyerhaeuser Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAXI SHIELDS?
The FDA product code for MAXI SHIELDS is HHD.
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 Weyerhaeuser Co. 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: HHD)
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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