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FDA 510(k)

THE SPRITZ BATH

K-Number: K912179 · 1991-08-28

ApplicantThe Spritz Co.
Decision Date1991-08-28
Product CodeKTC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE SPRITZ BATH is the device name listed in this FDA 510(k) record. The listed applicant is The Spritz Co.. It received FDA 510(k) clearance on 1991-08-28 under 510(k) number K912179. 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 THE SPRITZ BATH?

THE SPRITZ BATH is a medical device that received FDA 510(k) clearance on 1991-08-28. The listed applicant is The Spritz Co.. The 510(k) number is K912179.

When did THE SPRITZ BATH receive FDA 510(k) clearance?

THE SPRITZ BATH received FDA 510(k) clearance on 1991-08-28, under 510(k) number K912179.

Who is the listed applicant for THE SPRITZ BATH?

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

What is the FDA product code for THE SPRITZ BATH?

The FDA product code for THE SPRITZ BATH is KTC.

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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.

K890085SIT-N-BATHE SITZ BATHDrummond Industries, Inc.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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