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)

CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900

K-Number: K091637 · 2009-09-29

ApplicantCorpak Medsystems
Decision Date2009-09-29
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900 is the device name listed in this FDA 510(k) record. The listed applicant is Corpak Medsystems. It received FDA 510(k) clearance on 2009-09-29 under 510(k) number K091637. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900?

CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900 is a medical device that received FDA 510(k) clearance on 2009-09-29. The listed applicant is Corpak Medsystems. The 510(k) number is K091637.

When did CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900 receive FDA 510(k) clearance?

CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900 received FDA 510(k) clearance on 2009-09-29, under 510(k) number K091637.

Who is the listed applicant for CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900?

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

What is the FDA product code for CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900?

The FDA product code for CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900 is KNT.

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 Corpak Medsystems 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.

K131532ELECTROMAGNETIC TRANSMITTING STYLETK113351CORTRAK ENTERAL ACCESS DEVICEK100365FARRELL VALVE WITH CORFLO ANTI-IV CONNECTORS MODEL 20-4300AIVK083776CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1030AIV-LB-SK083791CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-SK083786CORFLO ANTI-IV ENTERAL FEEDING EXTENSION SET, MODELS 20-1006AIV-LB AND 20-1030AIV-LB

View all 13 devices →

Related Devices (Code: KNT)

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.

K26189052Fr ViSiGi LUX™; 52Fr ViSiGi 3D®Boehringer Laboratories, LLCK253514Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220); Blakemore Esophageal-Nasogastric Tube - 20 French (0092100); Blakemore Esophageal-Nasogastric Tube - 16 French (0092300)C.R. Bard, Inc.K250389XNY Disposable Gastric Calibration TubeChangzhou Xin Neng Yuan Medical Stapler Co.,LtdK243228Flexi-Seal AIR (with ENFit Connector)ConvatecK242336hygh-tec Drainage IIAmb MedtecK242901ZZIREN™ Orogastric Tube; ZZIREN™ SGT Orogastric Tube - 32 Fr (ZZ-SGT-32); ZZIREN™ SGT Orogastric Tube - 36 Fr (ZZ-SGT-36); ZZIREN™ SGT Orogastric Tube - 40 Fr (ZZ-SGT-40); ZZIREN™ GBT Orogastric Tube - 32 Fr (ZZ-GBT-32); ZZIREN™ GBT Orogastric Tube - 36 Fr (ZZ-GBT-36); ZZIREN™ GBT Orogastric Tube - 40 Fr (ZZ-GBT-40)Tools For Surgery, LLC

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.

↑