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FDA 510(k)

SHOWER STOOL W/HANDLES

K-Number: K830852 · 1983-04-05

ApplicantLic-Orthion
Decision Date1983-04-05
Product CodeILS
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SHOWER STOOL W/HANDLES is the device name listed in this FDA 510(k) record. The listed applicant is Lic-Orthion. It received FDA 510(k) clearance on 1983-04-05 under 510(k) number K830852. 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 SHOWER STOOL W/HANDLES?

SHOWER STOOL W/HANDLES is a medical device that received FDA 510(k) clearance on 1983-04-05. The listed applicant is Lic-Orthion. The 510(k) number is K830852.

When did SHOWER STOOL W/HANDLES receive FDA 510(k) clearance?

SHOWER STOOL W/HANDLES received FDA 510(k) clearance on 1983-04-05, under 510(k) number K830852.

Who is the listed applicant for SHOWER STOOL W/HANDLES?

The FDA 510(k) record lists Lic-Orthion as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHOWER STOOL W/HANDLES?

The FDA product code for SHOWER STOOL W/HANDLES 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 Lic-Orthion 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.

View all 17 devices →

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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