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FDA 510(k)

PERCUTANEOUS GASTROINTESTINAL TUBE

K-Number: K810499 · 1981-03-04

ApplicantHealth Development Corp.
Decision Date1981-03-04
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS GASTROINTESTINAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Health Development Corp.. It received FDA 510(k) clearance on 1981-03-04 under 510(k) number K810499. 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 PERCUTANEOUS GASTROINTESTINAL TUBE?

PERCUTANEOUS GASTROINTESTINAL TUBE is a medical device that received FDA 510(k) clearance on 1981-03-04. The listed applicant is Health Development Corp.. The 510(k) number is K810499.

When did PERCUTANEOUS GASTROINTESTINAL TUBE receive FDA 510(k) clearance?

PERCUTANEOUS GASTROINTESTINAL TUBE received FDA 510(k) clearance on 1981-03-04, under 510(k) number K810499.

Who is the listed applicant for PERCUTANEOUS GASTROINTESTINAL TUBE?

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

What is the FDA product code for PERCUTANEOUS GASTROINTESTINAL TUBE?

The FDA product code for PERCUTANEOUS GASTROINTESTINAL TUBE is KNT.

Related Clinical Trials

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Other records listing Health Development 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.

K830397PEM-CK823937SEMINAL COLLECTION DEVICEK802482KEOFEED (R) EASY-FILL ENTERIC FEED BAGK791714SURGIFEED

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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