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FDA 510(k)

PORTABLE SHOWER BATH

K-Number: K823327 · 1982-12-07

ApplicantWall Manufacturer, Inc.
Decision Date1982-12-07
Product CodeILM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PORTABLE SHOWER BATH is the device name listed in this FDA 510(k) record. The listed applicant is Wall Manufacturer, Inc.. It received FDA 510(k) clearance on 1982-12-07 under 510(k) number K823327. The device is classified under product code ILM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTABLE SHOWER BATH?

PORTABLE SHOWER BATH is a medical device that received FDA 510(k) clearance on 1982-12-07. The listed applicant is Wall Manufacturer, Inc.. The 510(k) number is K823327.

When did PORTABLE SHOWER BATH receive FDA 510(k) clearance?

PORTABLE SHOWER BATH received FDA 510(k) clearance on 1982-12-07, under 510(k) number K823327.

Who is the listed applicant for PORTABLE SHOWER BATH?

The FDA 510(k) record lists Wall Manufacturer, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTABLE SHOWER BATH?

The FDA product code for PORTABLE SHOWER BATH is ILM.

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Related Devices (Code: ILM)

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.

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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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