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FDA 510(k)

CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S

K-Number: K083791 · 2009-03-04

Decision Date2009-03-04
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S is the device name listed in this FDA 510(k) record. The listed applicant is Corpak Medsystems. It received FDA 510(k) clearance on 2009-03-04 under 510(k) number K083791. 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 CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S?

CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S is a medical device that received FDA 510(k) clearance on 2009-03-04. The listed applicant is Corpak Medsystems. The 510(k) number is K083791.

When did CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S receive FDA 510(k) clearance?

CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S received FDA 510(k) clearance on 2009-03-04, under 510(k) number K083791.

Who is the listed applicant for CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S?

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 CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S?

The FDA product code for CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S 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.

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.

View all 13 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.

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.

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