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FDA 510(k)

SILVERSEAL WOUND PACKING STRIPS WITH X-STATIC

K-Number: K063190 · 2007-08-21

Decision Date2007-08-21
Product CodeQSY
DecisionSubstantially Equivalent

Device Summary

SILVERSEAL WOUND PACKING STRIPS WITH X-STATIC is the device name listed in this FDA 510(k) record. The listed applicant is Noble Fiber Technologies, Inc.. It received FDA 510(k) clearance on 2007-08-21 under 510(k) number K063190. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILVERSEAL WOUND PACKING STRIPS WITH X-STATIC?

SILVERSEAL WOUND PACKING STRIPS WITH X-STATIC is a medical device that received FDA 510(k) clearance on 2007-08-21. The listed applicant is Noble Fiber Technologies, Inc.. The 510(k) number is K063190.

When did SILVERSEAL WOUND PACKING STRIPS WITH X-STATIC receive FDA 510(k) clearance?

SILVERSEAL WOUND PACKING STRIPS WITH X-STATIC received FDA 510(k) clearance on 2007-08-21, under 510(k) number K063190.

Who is the listed applicant for SILVERSEAL WOUND PACKING STRIPS 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 WOUND PACKING STRIPS WITH X-STATIC?

The FDA product code for SILVERSEAL WOUND PACKING STRIPS WITH X-STATIC is QSY.

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: QSY)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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