Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

URINE COLLECTION BAG TYPE AP2090V

K-Number: K802733 · 1980-12-18

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

Device Summary

URINE COLLECTION BAG TYPE AP2090V 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 K802733. 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 AP2090V?

URINE COLLECTION BAG TYPE AP2090V 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 K802733.

When did URINE COLLECTION BAG TYPE AP2090V receive FDA 510(k) clearance?

URINE COLLECTION BAG TYPE AP2090V received FDA 510(k) clearance on 1980-12-18, under 510(k) number K802733.

Who is the listed applicant for URINE COLLECTION BAG TYPE AP2090V?

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 AP2090V?

The FDA product code for URINE COLLECTION BAG TYPE AP2090V 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K802734URINE COLLECTION BAG TYPE 710K802739URINE COLLECTION BAG TYPE 710APK802736URINE COOLECTION BAG TYPE 2090VK802738URINE COLLECTION BAG TYPE 1505VK802732URINE COLLECTION BAG TYPE AP2132VK802737URINE COLLECTION BAG TYPE 1590V

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.

K110518IBAGFuture Path Medical, LLCK9733644L DRAINAGE BAG, 4L BAG FOR PERITONEAL DIALYSIS, 4L URINARY DRAINAGE BAGMaersk Medical A/SK972887MEDLINE PREMIUM LEG BAG, MEDLINE FABRIC BAC LEG BAG, MEDLINE URINARY LEG BAGMedline Industries, Inc.K971271BESECURE EXTERNAL URINARY COLLECTION SYSTEMUrology Research Intl., Inc.K971929AMSINO URINARY LEG BAGAmsino Intl., Inc.K971764WELCON HUE-VU URINARY DRAINAGE BAGWelcon, Inc.

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.

↑