SILVERSEAL SILVERAID WITH X-STATIC
K-Number: K050726 · 2005-12-05
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Device Summary
Frequently Asked Questions
What is the SILVERSEAL SILVERAID WITH X-STATIC?
SILVERSEAL SILVERAID WITH X-STATIC is a medical device that received FDA 510(k) clearance on 2005-12-05. The listed applicant is Noble Fiber Technologies, Inc.. The 510(k) number is K050726.
When did SILVERSEAL SILVERAID WITH X-STATIC receive FDA 510(k) clearance?
SILVERSEAL SILVERAID WITH X-STATIC received FDA 510(k) clearance on 2005-12-05, under 510(k) number K050726.
Who is the listed applicant for SILVERSEAL SILVERAID WITH X-STATIC?
The FDA 510(k) record lists Noble Fiber Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SILVERSEAL SILVERAID WITH X-STATIC?
The FDA product code for SILVERSEAL SILVERAID WITH X-STATIC is FRO. This falls under the Anesthesiology category.
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 Noble Fiber Technologies, 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: FRO)
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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