CONTAIN X-RAY DETECTABLE LAP SPONGE
K-Number: K801768 · 1980-08-20
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Device Summary
Frequently Asked Questions
What is the CONTAIN X-RAY DETECTABLE LAP SPONGE?
CONTAIN X-RAY DETECTABLE LAP SPONGE is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is The Buckeye Cellulose Corp.. The 510(k) number is K801768.
When did CONTAIN X-RAY DETECTABLE LAP SPONGE receive FDA 510(k) clearance?
CONTAIN X-RAY DETECTABLE LAP SPONGE received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801768.
Who is the listed applicant for CONTAIN X-RAY DETECTABLE LAP SPONGE?
The FDA 510(k) record lists The Buckeye Cellulose Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTAIN X-RAY DETECTABLE LAP SPONGE?
The FDA product code for CONTAIN X-RAY DETECTABLE LAP SPONGE 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 The Buckeye Cellulose 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: 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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