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FDA 510(k)

KIM NASO-INTESTINAL TUBE

K-Number: K882918 · 1988-12-05

ApplicantSheridan Catheter Corp.
Decision Date1988-12-05
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KIM NASO-INTESTINAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Sheridan Catheter Corp.. It received FDA 510(k) clearance on 1988-12-05 under 510(k) number K882918. 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 KIM NASO-INTESTINAL TUBE?

KIM NASO-INTESTINAL TUBE is a medical device that received FDA 510(k) clearance on 1988-12-05. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K882918.

When did KIM NASO-INTESTINAL TUBE receive FDA 510(k) clearance?

KIM NASO-INTESTINAL TUBE received FDA 510(k) clearance on 1988-12-05, under 510(k) number K882918.

Who is the listed applicant for KIM NASO-INTESTINAL TUBE?

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

What is the FDA product code for KIM NASO-INTESTINAL TUBE?

The FDA product code for KIM NASO-INTESTINAL TUBE is KNT.

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Other records listing Sheridan Catheter 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.

K922894LAZER-TRACH TRACHEAL TUBEK897046LASER RESISTANT TRACHEAL TUBEK890823ACCESSORY TO CLINICAL ELECTRONIC THERMOMETERK884765CLINICAL ELECTRONIC THERMOMETERSK882127CLINICAL ELECTRONIC THERMOMETERSK881368CLINICAL ELECTONIC THERMOMETERS

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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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