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FDA 510(k)

URINE COLLECTION BAG TYPE AP2132V

K-Number: K802732 · 1980-12-18

ApplicantBio D Corp.
Decision Date1980-12-18
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URINE COLLECTION BAG TYPE AP2132V is the device name listed in this FDA 510(k) record. The listed applicant is Bio D Corp.. It received FDA 510(k) clearance on 1980-12-18 under 510(k) number K802732. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINE COLLECTION BAG TYPE AP2132V?

URINE COLLECTION BAG TYPE AP2132V 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 K802732.

When did URINE COLLECTION BAG TYPE AP2132V receive FDA 510(k) clearance?

URINE COLLECTION BAG TYPE AP2132V received FDA 510(k) clearance on 1980-12-18, under 510(k) number K802732.

Who is the listed applicant for URINE COLLECTION BAG TYPE AP2132V?

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 AP2132V?

The FDA product code for URINE COLLECTION BAG TYPE AP2132V 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.

View all 11 devices →

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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