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FDA 510(k)

RADIUS ENTERAL FEEDING TUBE

K-Number: K930510 · 1995-02-01

ApplicantRadius Intl., Inc.
Decision Date1995-02-01
Product CodeBSS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RADIUS ENTERAL FEEDING TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Radius Intl., Inc.. It received FDA 510(k) clearance on 1995-02-01 under 510(k) number K930510. The device is classified under product code BSS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIUS ENTERAL FEEDING TUBE?

RADIUS ENTERAL FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1995-02-01. The listed applicant is Radius Intl., Inc.. The 510(k) number is K930510.

When did RADIUS ENTERAL FEEDING TUBE receive FDA 510(k) clearance?

RADIUS ENTERAL FEEDING TUBE received FDA 510(k) clearance on 1995-02-01, under 510(k) number K930510.

Who is the listed applicant for RADIUS ENTERAL FEEDING TUBE?

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

What is the FDA product code for RADIUS ENTERAL FEEDING TUBE?

The FDA product code for RADIUS ENTERAL FEEDING TUBE is BSS.

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 Radius Intl., 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.

K972102RADIUS PUSH OVER THE GUIDE WIRE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KITK972025RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KITK971901RADIUS LOW PROFILE GASTROSTOMY TUBE KITK951560RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS)

Related Devices (Code: BSS)

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.

K051480ENTERAL FEEDING TUBEBiosearch Medical Products, Inc.K984629MOSS TUBES, INC. NASAL TUBE - MARK IVMoss Tubes, Inc.K961711ASPISAFE GASTRIC TUBEB.Braun Medical, Inc.K933596GASTRIC, CATHETER, IRRIGATION & ASPIRATIONPolamedco, Inc.K935688AN-10S ANDERSEN TUBE WITH STYLETH.W. Andersen Products, Inc.K934348TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FRTri-Med Specialties, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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