SAXON WET LUBE
K-Number: K900358 · 1990-04-02
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Device Summary
Frequently Asked Questions
What is the SAXON WET LUBE?
SAXON WET LUBE is a medical device that received FDA 510(k) clearance on 1990-04-02. The listed applicant is Safetex Corp.. The 510(k) number is K900358.
When did SAXON WET LUBE receive FDA 510(k) clearance?
SAXON WET LUBE received FDA 510(k) clearance on 1990-04-02, under 510(k) number K900358.
Who is the listed applicant for SAXON WET LUBE?
The FDA 510(k) record lists Safetex Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAXON WET LUBE?
The FDA product code for SAXON WET LUBE is HIS.
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 Safetex Corp. 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: HIS)
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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