URINE COLLECTION BAG TYPE 1505V
K-Number: K802738 · 1980-12-18
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Device Summary
Frequently Asked Questions
What is the URINE COLLECTION BAG TYPE 1505V?
URINE COLLECTION BAG TYPE 1505V is a medical device that received FDA 510(k) clearance on 1980-12-18. The listed applicant is Bio D Corp.. The 510(k) number is K802738.
When did URINE COLLECTION BAG TYPE 1505V receive FDA 510(k) clearance?
URINE COLLECTION BAG TYPE 1505V received FDA 510(k) clearance on 1980-12-18, under 510(k) number K802738.
Who is the listed applicant for URINE COLLECTION BAG TYPE 1505V?
The FDA 510(k) record lists Bio D Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URINE COLLECTION BAG TYPE 1505V?
The FDA product code for URINE COLLECTION BAG TYPE 1505V 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 Bio D Corp. 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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