ARM SLING, POUCH TYPE
K-Number: K812477 · 1981-09-14
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Device Summary
Frequently Asked Questions
What is the ARM SLING, POUCH TYPE?
ARM SLING, POUCH TYPE is a medical device that received FDA 510(k) clearance on 1981-09-14. The listed applicant is Maddak, Inc.. The 510(k) number is K812477.
When did ARM SLING, POUCH TYPE receive FDA 510(k) clearance?
ARM SLING, POUCH TYPE received FDA 510(k) clearance on 1981-09-14, under 510(k) number K812477.
Who is the listed applicant for ARM SLING, POUCH TYPE?
The FDA 510(k) record lists Maddak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARM SLING, POUCH TYPE?
The FDA product code for ARM SLING, POUCH TYPE is ILI.
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 Maddak, 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: ILI)
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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