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FDA 510(k)

ENTERAL PUMP SETS FOR USE WITH ROSS FLEXIFLO-III

K-Number: K895933 · 1990-05-02

ApplicantDelmed, Inc.
Decision Date1990-05-02
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTERAL PUMP SETS FOR USE WITH ROSS FLEXIFLO-III is the device name listed in this FDA 510(k) record. The listed applicant is Delmed, Inc.. It received FDA 510(k) clearance on 1990-05-02 under 510(k) number K895933. 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 ENTERAL PUMP SETS FOR USE WITH ROSS FLEXIFLO-III?

ENTERAL PUMP SETS FOR USE WITH ROSS FLEXIFLO-III is a medical device that received FDA 510(k) clearance on 1990-05-02. The listed applicant is Delmed, Inc.. The 510(k) number is K895933.

When did ENTERAL PUMP SETS FOR USE WITH ROSS FLEXIFLO-III receive FDA 510(k) clearance?

ENTERAL PUMP SETS FOR USE WITH ROSS FLEXIFLO-III received FDA 510(k) clearance on 1990-05-02, under 510(k) number K895933.

Who is the listed applicant for ENTERAL PUMP SETS FOR USE WITH ROSS FLEXIFLO-III?

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

What is the FDA product code for ENTERAL PUMP SETS FOR USE WITH ROSS FLEXIFLO-III?

The FDA product code for ENTERAL PUMP SETS FOR USE WITH ROSS FLEXIFLO-III is KNT.

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Other records listing Delmed, 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.

K895329600ML AND 1200ML ENTERAL BAG ADM. SET FOR ENTERAK895142ENTERAL PUMP SET WITH ENTERAL SPIKEK895650ENTERAL PUMP SET W/ENTERA-FLO SPIKEK894506ENTERA-FLO ENTERAL FEEDING PUMPK901478DELMED 80/2 DIALYSIS SYSTEM W/LAST BAG OPTIONK901477DELMED 80/2 DIALYSIS SYSTEM W/ULTRAFILTRATION

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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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