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FDA 510(k)

TONSIL SPONGE, X-RAY DETECTABLE, W/STRING

K-Number: K882709 · 1988-08-03

ApplicantBioseal
Decision Date1988-08-03
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TONSIL SPONGE, X-RAY DETECTABLE, W/STRING is the device name listed in this FDA 510(k) record. The listed applicant is Bioseal. It received FDA 510(k) clearance on 1988-08-03 under 510(k) number K882709. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 10 devices →

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

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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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