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FDA 510(k)

KAYE MODEL KIAO PELVIC/THIGH STABILIZER

K-Number: K923095 · 1992-07-21

Decision Date1992-07-21
Product CodeINN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KAYE MODEL KIAO PELVIC/THIGH STABILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Kaye Products, Inc.. It received FDA 510(k) clearance on 1992-07-21 under 510(k) number K923095. 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 KAYE MODEL KIAO PELVIC/THIGH STABILIZER?

KAYE MODEL KIAO PELVIC/THIGH STABILIZER is a medical device that received FDA 510(k) clearance on 1992-07-21. The listed applicant is Kaye Products, Inc.. The 510(k) number is K923095.

When did KAYE MODEL KIAO PELVIC/THIGH STABILIZER receive FDA 510(k) clearance?

KAYE MODEL KIAO PELVIC/THIGH STABILIZER received FDA 510(k) clearance on 1992-07-21, under 510(k) number K923095.

Who is the listed applicant for KAYE MODEL KIAO PELVIC/THIGH STABILIZER?

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

What is the FDA product code for KAYE MODEL KIAO PELVIC/THIGH STABILIZER?

The FDA product code for KAYE MODEL KIAO PELVIC/THIGH STABILIZER 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.

Other records listing Kaye Products, 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.

View all 12 devices →

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

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