DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION
K-Number: K934299 · 1994-02-14
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Device Summary
Frequently Asked Questions
What is the DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION?
DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-02-14. The listed applicant is Smith & Nephew Dyonics, Inc.. The 510(k) number is K934299.
When did DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION receive FDA 510(k) clearance?
DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION received FDA 510(k) clearance on 1994-02-14, under 510(k) number K934299.
Who is the listed applicant for DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION?
The FDA 510(k) record lists Smith & Nephew Dyonics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION?
The FDA product code for DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION is HRX.
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 Smith & Nephew Dyonics, 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: HRX)
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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