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FDA 510(k)

SIT-N-BATHE SITZ BATH

K-Number: K890085 · 1989-02-13

ApplicantDrummond Industries, Inc.
Decision Date1989-02-13
Product CodeKTC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SIT-N-BATHE SITZ BATH is the device name listed in this FDA 510(k) record. The listed applicant is Drummond Industries, Inc.. It received FDA 510(k) clearance on 1989-02-13 under 510(k) number K890085. The device is classified under product code KTC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIT-N-BATHE SITZ BATH?

SIT-N-BATHE SITZ BATH is a medical device that received FDA 510(k) clearance on 1989-02-13. The listed applicant is Drummond Industries, Inc.. The 510(k) number is K890085.

When did SIT-N-BATHE SITZ BATH receive FDA 510(k) clearance?

SIT-N-BATHE SITZ BATH received FDA 510(k) clearance on 1989-02-13, under 510(k) number K890085.

Who is the listed applicant for SIT-N-BATHE SITZ BATH?

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

What is the FDA product code for SIT-N-BATHE SITZ BATH?

The FDA product code for SIT-N-BATHE SITZ BATH is KTC.

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.

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Related Devices (Code: KTC)

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.

K912179THE SPRITZ BATHThe Spritz Co.K862600SITZ BATHW. C. Green, D.D.S.K851309ABCO PLASTIC UTENSILSAbco Dealers, Inc.K841711MAC LEE SITZ BATHMac Lee Medical ProductsK831762SITZ BATH, SINGLE PATIENT USE #8100Lsl Industries, Inc.K800958PERSONAL SITZ BATH KITThe Healthcare Group Laboratories, Inc.

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.

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