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FDA 510(k)

IMPROVED BAKER TWIN-CUFF SUMP TUBE

K-Number: K901683 · 1990-06-27

ApplicantBissell Medical Products, Inc.
Decision Date1990-06-27
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

IMPROVED BAKER TWIN-CUFF SUMP TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Bissell Medical Products, Inc.. It received FDA 510(k) clearance on 1990-06-27 under 510(k) number K901683. 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 IMPROVED BAKER TWIN-CUFF SUMP TUBE?

IMPROVED BAKER TWIN-CUFF SUMP TUBE is a medical device that received FDA 510(k) clearance on 1990-06-27. The listed applicant is Bissell Medical Products, Inc.. The 510(k) number is K901683.

When did IMPROVED BAKER TWIN-CUFF SUMP TUBE receive FDA 510(k) clearance?

IMPROVED BAKER TWIN-CUFF SUMP TUBE received FDA 510(k) clearance on 1990-06-27, under 510(k) number K901683.

Who is the listed applicant for IMPROVED BAKER TWIN-CUFF SUMP TUBE?

The FDA 510(k) record lists Bissell Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPROVED BAKER TWIN-CUFF SUMP TUBE?

The FDA product code for IMPROVED BAKER TWIN-CUFF SUMP TUBE is KNT.

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Other records listing Bissell Medical Products, 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.

K932880GRASSI GASTROJEJUNOSTOMY TUBEK914140GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEEDK873441BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBEK871691MODIFIED MULTI-LUMEN NASOGASTRIC TUBEK851672NYHUS/NELSON TUBE

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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