URINE COLLECTION BAG TYPE 710
K-Number: K802734 · 1980-12-18
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Device Summary
Frequently Asked Questions
What is the URINE COLLECTION BAG TYPE 710?
URINE COLLECTION BAG TYPE 710 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 K802734.
When did URINE COLLECTION BAG TYPE 710 receive FDA 510(k) clearance?
URINE COLLECTION BAG TYPE 710 received FDA 510(k) clearance on 1980-12-18, under 510(k) number K802734.
Who is the listed applicant for URINE COLLECTION BAG TYPE 710?
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 710?
The FDA product code for URINE COLLECTION BAG TYPE 710 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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