PROSYS LEG BAG
K-Number: K952208 · 1995-08-15
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Device Summary
Frequently Asked Questions
What is the PROSYS LEG BAG?
PROSYS LEG BAG is a medical device that received FDA 510(k) clearance on 1995-08-15. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K952208.
When did PROSYS LEG BAG receive FDA 510(k) clearance?
PROSYS LEG BAG received FDA 510(k) clearance on 1995-08-15, under 510(k) number K952208.
Who is the listed applicant for PROSYS LEG BAG?
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 PROSYS LEG BAG?
The FDA product code for PROSYS LEG BAG 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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