ACCUSEAL LEG BAGS & EXTENSION TUBES
K-Number: K842396 · 1984-08-08
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Device Summary
Frequently Asked Questions
What is the ACCUSEAL LEG BAGS & EXTENSION TUBES?
ACCUSEAL LEG BAGS & EXTENSION TUBES is a medical device that received FDA 510(k) clearance on 1984-08-08. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K842396.
When did ACCUSEAL LEG BAGS & EXTENSION TUBES receive FDA 510(k) clearance?
ACCUSEAL LEG BAGS & EXTENSION TUBES received FDA 510(k) clearance on 1984-08-08, under 510(k) number K842396.
Who is the listed applicant for ACCUSEAL LEG BAGS & EXTENSION TUBES?
The FDA 510(k) record lists Convatec, A Division of E.R. Squibb & Sons as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACCUSEAL LEG BAGS & EXTENSION TUBES?
The FDA product code for ACCUSEAL LEG BAGS & EXTENSION TUBES is KNX.
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 Convatec, A Division of E.R. Squibb & Sons 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: KNX)
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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