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FDA 510(k)

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT

K-Number: K885220 · 1989-09-25

ApplicantEthox Corp.
Decision Date1989-09-25
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ethox Corp.. It received FDA 510(k) clearance on 1989-09-25 under 510(k) number K885220. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT?

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT is a medical device that received FDA 510(k) clearance on 1989-09-25. The listed applicant is Ethox Corp.. The 510(k) number is K885220.

When did PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT receive FDA 510(k) clearance?

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT received FDA 510(k) clearance on 1989-09-25, under 510(k) number K885220.

Who is the listed applicant for PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT?

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

What is the FDA product code for PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT?

The FDA product code for PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT is KNT.

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Other records listing Ethox Corp. 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.

K040286ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFSK031195CUF-COVER (TM)K962850TUM-E-VACK935633NO-MESK921946TUM-E-VAC BITE BLOCKK894927SURGI SQUEEZ

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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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