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FDA 510(k)

RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE)

K-Number: K973892 · 1998-05-18

ApplicantRusch Intl.
Decision Date1998-05-18
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE) is the device name listed in this FDA 510(k) record. The listed applicant is Rusch Intl.. It received FDA 510(k) clearance on 1998-05-18 under 510(k) number K973892. 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 RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE)?

RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE) is a medical device that received FDA 510(k) clearance on 1998-05-18. The listed applicant is Rusch Intl.. The 510(k) number is K973892.

When did RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE) receive FDA 510(k) clearance?

RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE) received FDA 510(k) clearance on 1998-05-18, under 510(k) number K973892.

Who is the listed applicant for RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE)?

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

What is the FDA product code for RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE)?

The FDA product code for RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE) is KNT.

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Other records listing Rusch Intl. 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.

K033023INTERMITTENT URETHRAL CATHETERSK030559RUSCH POLYFLEX STENT FOR THE ESOPHAGUS W/INTRODUCER/DELIVERY SYSTEMK023666RUSCH GUIDED CHOLANGIOGRAPHY CATHETERK023918RUSCH CRYSTAL CLEAR TRACHEOSTOMY SETS, CUFFED AND CUFFLESSK023964RUSCH MICROLARYNGEAL TUBEK021540RUSCH EDGAR 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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