GARELICK COMMODE
K-Number: K802511 · 1980-11-12
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Device Summary
Frequently Asked Questions
What is the GARELICK COMMODE?
GARELICK COMMODE is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Garelick Mfg. Co.. The 510(k) number is K802511.
When did GARELICK COMMODE receive FDA 510(k) clearance?
GARELICK COMMODE received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802511.
Who is the listed applicant for GARELICK COMMODE?
The FDA 510(k) record lists Garelick Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GARELICK COMMODE?
The FDA product code for GARELICK COMMODE 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.
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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