URINARY DRAINAGE UNIT
K-Number: K890551 · 1989-02-28
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Device Summary
Frequently Asked Questions
What is the URINARY DRAINAGE UNIT?
URINARY DRAINAGE UNIT is a medical device that received FDA 510(k) clearance on 1989-02-28. The listed applicant is Consolidated Products & Services, Inc.. The 510(k) number is K890551.
When did URINARY DRAINAGE UNIT receive FDA 510(k) clearance?
URINARY DRAINAGE UNIT received FDA 510(k) clearance on 1989-02-28, under 510(k) number K890551.
Who is the listed applicant for URINARY DRAINAGE UNIT?
The FDA 510(k) record lists Consolidated Products & Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URINARY DRAINAGE UNIT?
The FDA product code for URINARY DRAINAGE UNIT 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 Consolidated Products & Services, Inc. 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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