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)

BOTTLE ADAPTER

K-Number: K830571 · 1983-03-24

ApplicantBurron Medical Products, Inc.
Decision Date1983-03-24
Product CodeKYX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOTTLE ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K830571. The device is classified under product code KYX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOTTLE ADAPTER?

BOTTLE ADAPTER is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K830571.

When did BOTTLE ADAPTER receive FDA 510(k) clearance?

BOTTLE ADAPTER received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830571.

Who is the listed applicant for BOTTLE ADAPTER?

The FDA 510(k) record lists Burron Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOTTLE ADAPTER?

The FDA product code for BOTTLE ADAPTER is KYX.

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 Burron Medical Products, Inc. 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.

K870403CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTUREK862412INTESTOPLANTK861479CAVAFIX, CENTRAL VENOUS CATHETER KITK860126STIMUPLEX, NERVE STIMULATORK851293IMPLANTOFIXK841428JEJUNOSTOMY SET FOR TUBE FEEDING

View all 41 devices →

Related Devices (Code: KYX)

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.

K980109CYCLOTECH CYCLOSPORINE ORAL SOLUTIONS DISPENSERSangstat Medical Corp.K954181CANYONS BI-DIRECTIONAL CHECK VALVECanyon Medical ProductsK801008MULTI-AD FLUID DISPENSING PUMP MP-3000Burron Medical Products, Inc.K800362FLUID DISPENSING SYSTEMPharmaseal LaboratoriesK800437SYRINGE TIP CONNECTORBurron Medical Products, Inc.K792227MULTI-AD FLUID DISPENSING SYSTEMNational Patent Development Corp.

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.

↑