KENDALL CURITY URINARY DRAINAGE BAGS
K-Number: K892433 · 1989-05-05
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Device Summary
Frequently Asked Questions
What is the KENDALL CURITY URINARY DRAINAGE BAGS?
KENDALL CURITY URINARY DRAINAGE BAGS is a medical device that received FDA 510(k) clearance on 1989-05-05. The listed applicant is The Kendal Co.. The 510(k) number is K892433.
When did KENDALL CURITY URINARY DRAINAGE BAGS receive FDA 510(k) clearance?
KENDALL CURITY URINARY DRAINAGE BAGS received FDA 510(k) clearance on 1989-05-05, under 510(k) number K892433.
Who is the listed applicant for KENDALL CURITY URINARY DRAINAGE BAGS?
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 KENDALL CURITY URINARY DRAINAGE BAGS?
The FDA product code for KENDALL CURITY URINARY DRAINAGE BAGS 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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