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)

INFANT FEEDING TUBE

K-Number: K953008 · 1996-01-11

ApplicantMarquette Medical, Inc.
Decision Date1996-01-11
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INFANT FEEDING TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Medical, Inc.. It received FDA 510(k) clearance on 1996-01-11 under 510(k) number K953008. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFANT FEEDING TUBE?

INFANT FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1996-01-11. The listed applicant is Marquette Medical, Inc.. The 510(k) number is K953008.

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

INFANT FEEDING TUBE received FDA 510(k) clearance on 1996-01-11, under 510(k) number K953008.

Who is the listed applicant for INFANT FEEDING TUBE?

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

What is the FDA product code for INFANT FEEDING TUBE?

The FDA product code for INFANT FEEDING TUBE is FPD.

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 Marquette Medical, 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.

K021471MARQUETTE HUBER TRAP SAFETY INFUSION SETK952976PLASTIC BLUNT CANNULAK920537SUBCUTANEOUS INFUSION SETK9052184 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMPK9052194' LOW VOLUME IV EXTENSION SETK905374IV EXTENSION SETS WITH .22 MICRON FILTER

View all 17 devices →

Related Devices (Code: FPD)

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.

K243361NutrifitVygon USAK180236VR Medical Feeding Tube and Enteral Feeding Extension Set (EFES)Vr Medical Technology Co., Ltd.K131590INNERSENSE ESOPHAGEAL TEMPERATURE PROBE / FEEDING TUBEPhilips Medical SystemsK120815INNERSENSE ESOPHAGEAL TEMPERATURE/FEEDING TUBEPhilips Medical SystemsK121105NUTRISAFE 2 FEEDING TUBEVygon Corp.K100163NUTRISAFE 2 FEEDING TUBES MODEL 362.XXX. 1362.XXXVygon 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.

↑