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FDA 510(k)

SHOWER CHAIRS

K-Number: K922045 · 1992-05-26

Decision Date1992-05-26
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SHOWER CHAIRS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Inspection Co., Inc.. It received FDA 510(k) clearance on 1992-05-26 under 510(k) number K922045. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHOWER CHAIRS?

SHOWER CHAIRS is a medical device that received FDA 510(k) clearance on 1992-05-26. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K922045.

When did SHOWER CHAIRS receive FDA 510(k) clearance?

SHOWER CHAIRS received FDA 510(k) clearance on 1992-05-26, under 510(k) number K922045.

Who is the listed applicant for SHOWER CHAIRS?

The FDA 510(k) record lists Medical Device Inspection Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHOWER CHAIRS?

The FDA product code for SHOWER CHAIRS is INM.

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 Medical Device Inspection 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.

View all 30 devices →

Related Devices (Code: INM)

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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