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FDA 510(k)

RPI ENTERAL FEEDING BAG 1000ML AND 500ML

K-Number: K902641 · 1990-10-01

Decision Date1990-10-01
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RPI ENTERAL FEEDING BAG 1000ML AND 500ML is the device name listed in this FDA 510(k) record. The listed applicant is Ridge Products, Inc.. It received FDA 510(k) clearance on 1990-10-01 under 510(k) number K902641. 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 RPI ENTERAL FEEDING BAG 1000ML AND 500ML?

RPI ENTERAL FEEDING BAG 1000ML AND 500ML is a medical device that received FDA 510(k) clearance on 1990-10-01. The listed applicant is Ridge Products, Inc.. The 510(k) number is K902641.

When did RPI ENTERAL FEEDING BAG 1000ML AND 500ML receive FDA 510(k) clearance?

RPI ENTERAL FEEDING BAG 1000ML AND 500ML received FDA 510(k) clearance on 1990-10-01, under 510(k) number K902641.

Who is the listed applicant for RPI ENTERAL FEEDING BAG 1000ML AND 500ML?

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

What is the FDA product code for RPI ENTERAL FEEDING BAG 1000ML AND 500ML?

The FDA product code for RPI ENTERAL FEEDING BAG 1000ML AND 500ML 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.

Other records listing Ridge 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.

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.

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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