FOREARM-CANE
K-Number: K790299 · 1979-02-21
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Device Summary
Frequently Asked Questions
What is the FOREARM-CANE?
FOREARM-CANE is a medical device that received FDA 510(k) clearance on 1979-02-21. The listed applicant is Guardian Products Co., Inc.. The 510(k) number is K790299.
When did FOREARM-CANE receive FDA 510(k) clearance?
FOREARM-CANE received FDA 510(k) clearance on 1979-02-21, under 510(k) number K790299.
Who is the listed applicant for FOREARM-CANE?
The FDA 510(k) record lists Guardian Products Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FOREARM-CANE?
The FDA product code for FOREARM-CANE is IPS.
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 Guardian Products Co., 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: IPS)
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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