TONSIL SPONGE, X-RAY DETECTABLE, W/STRING
K-Number: K882709 · 1988-08-03
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Device Summary
Frequently Asked Questions
What is the TONSIL SPONGE, X-RAY DETECTABLE, W/STRING?
TONSIL SPONGE, X-RAY DETECTABLE, W/STRING is a medical device that received FDA 510(k) clearance on 1988-08-03. The listed applicant is Bioseal. The 510(k) number is K882709.
When did TONSIL SPONGE, X-RAY DETECTABLE, W/STRING receive FDA 510(k) clearance?
TONSIL SPONGE, X-RAY DETECTABLE, W/STRING received FDA 510(k) clearance on 1988-08-03, under 510(k) number K882709.
Who is the listed applicant for TONSIL SPONGE, X-RAY DETECTABLE, W/STRING?
The FDA 510(k) record lists Bioseal as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TONSIL SPONGE, X-RAY DETECTABLE, W/STRING?
The FDA product code for TONSIL SPONGE, X-RAY DETECTABLE, W/STRING is GDY.
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 Bioseal 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: GDY)
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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