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FDA 510(k)

SHOWER-A-WAY

K-Number: K902951 · 1990-07-25

Decision Date1990-07-25
Product CodeINN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SHOWER-A-WAY is the device name listed in this FDA 510(k) record. The listed applicant is Tri-S-Sales and Mfg.. It received FDA 510(k) clearance on 1990-07-25 under 510(k) number K902951. The device is classified under product code INN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHOWER-A-WAY?

SHOWER-A-WAY is a medical device that received FDA 510(k) clearance on 1990-07-25. The listed applicant is Tri-S-Sales and Mfg.. The 510(k) number is K902951.

When did SHOWER-A-WAY receive FDA 510(k) clearance?

SHOWER-A-WAY received FDA 510(k) clearance on 1990-07-25, under 510(k) number K902951.

Who is the listed applicant for SHOWER-A-WAY?

The FDA 510(k) record lists Tri-S-Sales and Mfg. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHOWER-A-WAY?

The FDA product code for SHOWER-A-WAY is INN.

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: INN)

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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