BATHTUB GRAB BAR
K-Number: K821009 · 1982-04-21
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Device Summary
Frequently Asked Questions
What is the BATHTUB GRAB BAR?
BATHTUB GRAB BAR is a medical device that received FDA 510(k) clearance on 1982-04-21. The listed applicant is Guardian Products Co., Inc.. The 510(k) number is K821009.
When did BATHTUB GRAB BAR receive FDA 510(k) clearance?
BATHTUB GRAB BAR received FDA 510(k) clearance on 1982-04-21, under 510(k) number K821009.
Who is the listed applicant for BATHTUB GRAB BAR?
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 BATHTUB GRAB BAR?
The FDA product code for BATHTUB GRAB BAR is ILS.
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: ILS)
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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