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FDA 510(k)

AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE

K-Number: K992719 · 2000-01-12

ApplicantAmsino Intl., Inc.
Decision Date2000-01-12
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE is the device name listed in this FDA 510(k) record. The listed applicant is Amsino Intl., Inc.. It received FDA 510(k) clearance on 2000-01-12 under 510(k) number K992719. 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 AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE?

AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE is a medical device that received FDA 510(k) clearance on 2000-01-12. The listed applicant is Amsino Intl., Inc.. The 510(k) number is K992719.

When did AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE receive FDA 510(k) clearance?

AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE received FDA 510(k) clearance on 2000-01-12, under 510(k) number K992719.

Who is the listed applicant for AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE?

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

What is the FDA product code for AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE?

The FDA product code for AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE is KNT.

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Other records listing Amsino Intl., 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.

K070873AMSURE BLADDER IRRIGATION SETK974042AMSURE CLEANSING ENEMA SETK973107AMSINO I.V. ADMINISTRATION SETK973199AMSINO SUCTION CATHETERK971929AMSINO URINARY LEG BAGK964745AMSINO URINARY DRAINAGE BAG

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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.

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