BOUNDARY SURGICAL DRAPE
K-Number: K812962 · 1981-11-20
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Device Summary
Frequently Asked Questions
What is the BOUNDARY SURGICAL DRAPE?
BOUNDARY SURGICAL DRAPE is a medical device that received FDA 510(k) clearance on 1981-11-20. The listed applicant is The Buckeye Cellulose Corp.. The 510(k) number is K812962.
When did BOUNDARY SURGICAL DRAPE receive FDA 510(k) clearance?
BOUNDARY SURGICAL DRAPE received FDA 510(k) clearance on 1981-11-20, under 510(k) number K812962.
Who is the listed applicant for BOUNDARY SURGICAL DRAPE?
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 BOUNDARY SURGICAL DRAPE?
The FDA product code for BOUNDARY SURGICAL DRAPE is KKX.
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: KKX)
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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