COX DISPOSABLE RETRIEVAL DEVICES
K-Number: K923489 · 1992-09-23
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Device Summary
Frequently Asked Questions
What is the COX DISPOSABLE RETRIEVAL DEVICES?
COX DISPOSABLE RETRIEVAL DEVICES is a medical device that received FDA 510(k) clearance on 1992-09-23. The listed applicant is Cox Medical Ent., Inc.. The 510(k) number is K923489.
When did COX DISPOSABLE RETRIEVAL DEVICES receive FDA 510(k) clearance?
COX DISPOSABLE RETRIEVAL DEVICES received FDA 510(k) clearance on 1992-09-23, under 510(k) number K923489.
Who is the listed applicant for COX DISPOSABLE RETRIEVAL DEVICES?
The FDA 510(k) record lists Cox Medical Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COX DISPOSABLE RETRIEVAL DEVICES?
The FDA product code for COX DISPOSABLE RETRIEVAL DEVICES is OCZ.
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 Cox Medical Ent., 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: OCZ)
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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