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FDA 510(k)

CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM

K-Number: K970178 · 1997-07-21

ApplicantCorpak, Inc.
Decision Date1997-07-21
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Corpak, Inc.. It received FDA 510(k) clearance on 1997-07-21 under 510(k) number K970178. 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 CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM?

CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM is a medical device that received FDA 510(k) clearance on 1997-07-21. The listed applicant is Corpak, Inc.. The 510(k) number is K970178.

When did CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM receive FDA 510(k) clearance?

CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM received FDA 510(k) clearance on 1997-07-21, under 510(k) number K970178.

Who is the listed applicant for CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM?

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

What is the FDA product code for CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM?

The FDA product code for CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM 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.

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Other records listing Corpak, 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.

K964514CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSISK944750CORFLO 300 PUMP

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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