FDA 510(k)

PORT-A-BATH

K-Number: K770294 · 1977-03-30

Decision Date1977-03-30

Product CodeILK

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

PORT-A-BATH is the device name listed in this FDA 510(k) record. The listed applicant is Kathco, Inc.. It received FDA 510(k) clearance on 1977-03-30 under 510(k) number K770294. The device is classified under product code ILK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORT-A-BATH?

PORT-A-BATH is a medical device that received FDA 510(k) clearance on 1977-03-30. The listed applicant is Kathco, Inc.. The 510(k) number is K770294.

When did PORT-A-BATH receive FDA 510(k) clearance?

PORT-A-BATH received FDA 510(k) clearance on 1977-03-30, under 510(k) number K770294.

Who is the listed applicant for PORT-A-BATH?

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

What is the FDA product code for PORT-A-BATH?

The FDA product code for PORT-A-BATH is ILK.

Related Devices (Code: ILK)

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

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