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FDA 510(k)

SITZ BATH, SINGLE PATIENT USE #8100

K-Number: K831762 · 1983-06-24

Decision Date1983-06-24
Product CodeKTC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SITZ BATH, SINGLE PATIENT USE #8100 is the device name listed in this FDA 510(k) record. The listed applicant is Lsl Industries, Inc.. It received FDA 510(k) clearance on 1983-06-24 under 510(k) number K831762. 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 SITZ BATH, SINGLE PATIENT USE #8100?

SITZ BATH, SINGLE PATIENT USE #8100 is a medical device that received FDA 510(k) clearance on 1983-06-24. The listed applicant is Lsl Industries, Inc.. The 510(k) number is K831762.

When did SITZ BATH, SINGLE PATIENT USE #8100 receive FDA 510(k) clearance?

SITZ BATH, SINGLE PATIENT USE #8100 received FDA 510(k) clearance on 1983-06-24, under 510(k) number K831762.

Who is the listed applicant for SITZ BATH, SINGLE PATIENT USE #8100?

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

What is the FDA product code for SITZ BATH, SINGLE PATIENT USE #8100?

The FDA product code for SITZ BATH, SINGLE PATIENT USE #8100 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.

Other records listing Lsl Industries, Inc. as applicant

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: 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.

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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