DYNAREX NON-WOVEN SPONGE
K-Number: K960388 · 1996-04-01
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Device Summary
Frequently Asked Questions
What is the DYNAREX NON-WOVEN SPONGE?
DYNAREX NON-WOVEN SPONGE is a medical device that received FDA 510(k) clearance on 1996-04-01. The listed applicant is Dynarex Corp.. The 510(k) number is K960388.
When did DYNAREX NON-WOVEN SPONGE receive FDA 510(k) clearance?
DYNAREX NON-WOVEN SPONGE received FDA 510(k) clearance on 1996-04-01, under 510(k) number K960388.
Who is the listed applicant for DYNAREX NON-WOVEN SPONGE?
The FDA 510(k) record lists Dynarex Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNAREX NON-WOVEN SPONGE?
The FDA product code for DYNAREX NON-WOVEN SPONGE is EFQ.
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 Dynarex 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: EFQ)
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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