KAYE MODEL KIAO PELVIC/THIGH STABILIZER
K-Number: K923095 · 1992-07-21
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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