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FDA 510(k)

GARELICK COMMODE

K-Number: K802511 · 1980-11-12

Decision Date1980-11-12
Product CodeILS
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GARELICK COMMODE is the device name listed in this FDA 510(k) record. The listed applicant is Garelick Mfg. Co.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802511. The device is classified under product code ILS. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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