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)

CHEMOTHERAPY CONTAINER

K-Number: K911576 · 1991-07-05

ApplicantBemis Mfg. Co.
Decision Date1991-07-05
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHEMOTHERAPY CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Bemis Mfg. Co.. It received FDA 510(k) clearance on 1991-07-05 under 510(k) number K911576. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEMOTHERAPY CONTAINER?

CHEMOTHERAPY CONTAINER is a medical device that received FDA 510(k) clearance on 1991-07-05. The listed applicant is Bemis Mfg. Co.. The 510(k) number is K911576.

When did CHEMOTHERAPY CONTAINER receive FDA 510(k) clearance?

CHEMOTHERAPY CONTAINER received FDA 510(k) clearance on 1991-07-05, under 510(k) number K911576.

Who is the listed applicant for CHEMOTHERAPY CONTAINER?

The FDA 510(k) record lists Bemis Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHEMOTHERAPY CONTAINER?

The FDA product code for CHEMOTHERAPY CONTAINER is KPE.

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 Bemis Mfg. Co. 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.

K020921NO-POKES NEEDLE SAFETY DEVICEK965248BEMIS TWO GALLON SHARPS CONTAINERK964858BEMIS TWO GALLON CHEMOTHERAPY CONTAINERK960525BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)K953797SHARPS DISPOSAL CONTAINERSK950340IGHT AND ELEVEN GALLON SHARPS AND CHEMOTHERAPY CONTAINERS

View all 12 devices →

Related Devices (Code: KPE)

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.

K252079Disposable Infusion Bag for Parenteral NutritionBeijing L&Z Medical Technology Development Co., Ltd.K251980ClaveQS™ BagIcu Medical, Inc.K251139KabiHelp® Uno; KabiHelp® Advance plusFresenius Kabi AGK252094eZSURE™ Empty Fluid ContainerEpic Medical Pte. , Ltd.K250459DMRX 100ml Empty Container Solution; DMRX 250ml Empty Container Solution; DMRX 500ml Empty Container Solution; DMRX 1000ml Empty Container SolutionTechnoflex Sas.K241442eZSURE™ Empty Fluid Container with ProSeal™ Injection SiteEpic Medical Pte. , Ltd.

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.

↑