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FDA 510(k)

600 OR 1200 ML. ENTERAL BAG ADMINISTRATION SET

K-Number: K901753 · 1990-06-01

ApplicantChartermed, Inc.
Decision Date1990-06-01
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

600 OR 1200 ML. ENTERAL BAG ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Chartermed, Inc.. It received FDA 510(k) clearance on 1990-06-01 under 510(k) number K901753. 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 600 OR 1200 ML. ENTERAL BAG ADMINISTRATION SET?

600 OR 1200 ML. ENTERAL BAG ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1990-06-01. The listed applicant is Chartermed, Inc.. The 510(k) number is K901753.

When did 600 OR 1200 ML. ENTERAL BAG ADMINISTRATION SET receive FDA 510(k) clearance?

600 OR 1200 ML. ENTERAL BAG ADMINISTRATION SET received FDA 510(k) clearance on 1990-06-01, under 510(k) number K901753.

Who is the listed applicant for 600 OR 1200 ML. ENTERAL BAG ADMINISTRATION SET?

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

What is the FDA product code for 600 OR 1200 ML. ENTERAL BAG ADMINISTRATION SET?

The FDA product code for 600 OR 1200 ML. ENTERAL BAG ADMINISTRATION SET is KNT.

Related Clinical Trials

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Other records listing Chartermed, 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.

K973103CHARTERMED TPN-EVA BAGSK902079ADMIXTURE CONTAINER FOR TOTAL PARENTERAL NUTRITIONK902464CHARTERMED EMPTY TPN CONTAINER - 100 ML CAPACITY

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

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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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