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FDA 510(k)

VIVONEX TUNGSTEN TIP TUBE PLACEMENT

K-Number: K821231 · 1982-05-10

ApplicantNorwich Eaton Pharmaceuticals, Inc.
Decision Date1982-05-10
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VIVONEX TUNGSTEN TIP TUBE PLACEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Norwich Eaton Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1982-05-10 under 510(k) number K821231. 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 VIVONEX TUNGSTEN TIP TUBE PLACEMENT?

VIVONEX TUNGSTEN TIP TUBE PLACEMENT is a medical device that received FDA 510(k) clearance on 1982-05-10. The listed applicant is Norwich Eaton Pharmaceuticals, Inc.. The 510(k) number is K821231.

When did VIVONEX TUNGSTEN TIP TUBE PLACEMENT receive FDA 510(k) clearance?

VIVONEX TUNGSTEN TIP TUBE PLACEMENT received FDA 510(k) clearance on 1982-05-10, under 510(k) number K821231.

Who is the listed applicant for VIVONEX TUNGSTEN TIP TUBE PLACEMENT?

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

What is the FDA product code for VIVONEX TUNGSTEN TIP TUBE PLACEMENT?

The FDA product code for VIVONEX TUNGSTEN TIP TUBE PLACEMENT is KNT.

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Other records listing Norwich Eaton Pharmaceuticals, 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.

K842841VIVONEX TUNG STEN TIP TUBEK831968VIVONEX TUNGSTEN TIP TUBE-BRAIDEDK831969VIVONEX TUNGSTEN TIP TUBE-WOUNDK831971VIVONEX TUNGSTEN TIP TUBE-TWISTED WIREK831970VIVONEX TUNGSTEN TIP TUBE-MONOFILA-K822516VIVONEX MASS GASTRASTOMY TUBE

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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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