CURITY BEDSIDE DRAINAGE BAG
K-Number: K813621 · 1982-02-12
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Device Summary
Frequently Asked Questions
What is the CURITY BEDSIDE DRAINAGE BAG?
CURITY BEDSIDE DRAINAGE BAG is a medical device that received FDA 510(k) clearance on 1982-02-12. The listed applicant is The Kendal Co.. The 510(k) number is K813621.
When did CURITY BEDSIDE DRAINAGE BAG receive FDA 510(k) clearance?
CURITY BEDSIDE DRAINAGE BAG received FDA 510(k) clearance on 1982-02-12, under 510(k) number K813621.
Who is the listed applicant for CURITY BEDSIDE DRAINAGE BAG?
The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CURITY BEDSIDE DRAINAGE BAG?
The FDA product code for CURITY BEDSIDE DRAINAGE 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 The Kendal Co. 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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