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FDA 510(k)

BOEHRINGER GASTRIC SIZING TUBE

K-Number: K130483 · 2013-03-28

ApplicantBoehringer Laboratories, LLC
Decision Date2013-03-28
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BOEHRINGER GASTRIC SIZING TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories, LLC. It received FDA 510(k) clearance on 2013-03-28 under 510(k) number K130483. 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 BOEHRINGER GASTRIC SIZING TUBE?

BOEHRINGER GASTRIC SIZING TUBE is a medical device that received FDA 510(k) clearance on 2013-03-28. The listed applicant is Boehringer Laboratories, LLC. The 510(k) number is K130483.

When did BOEHRINGER GASTRIC SIZING TUBE receive FDA 510(k) clearance?

BOEHRINGER GASTRIC SIZING TUBE received FDA 510(k) clearance on 2013-03-28, under 510(k) number K130483.

Who is the listed applicant for BOEHRINGER GASTRIC SIZING TUBE?

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

What is the FDA product code for BOEHRINGER GASTRIC SIZING TUBE?

The FDA product code for BOEHRINGER GASTRIC SIZING TUBE is KNT.

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Other records listing Boehringer Laboratories, LLC 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.

K26189052Fr ViSiGi LUX™; 52Fr ViSiGi 3D®K243399Boehringer Laboratories Liver RetractorK234033ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)

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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