NASAL-SINUS PACKING
K-Number: K924542 · 1993-02-12
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Device Summary
Frequently Asked Questions
What is the NASAL-SINUS PACKING?
NASAL-SINUS PACKING is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Ultracell Medical Technologies, Inc.. The 510(k) number is K924542.
When did NASAL-SINUS PACKING receive FDA 510(k) clearance?
NASAL-SINUS PACKING received FDA 510(k) clearance on 1993-02-12, under 510(k) number K924542.
Who is the listed applicant for NASAL-SINUS PACKING?
The FDA 510(k) record lists Ultracell Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NASAL-SINUS PACKING?
The FDA product code for NASAL-SINUS PACKING is EMX.
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 Ultracell Medical 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: EMX)
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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