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FDA 510(k)

MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION

K-Number: K921370 · 1994-05-02

ApplicantMedical Innovations Corp.
Decision Date1994-05-02
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Medical Innovations Corp.. It received FDA 510(k) clearance on 1994-05-02 under 510(k) number K921370. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION?

MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-05-02. The listed applicant is Medical Innovations Corp.. The 510(k) number is K921370.

When did MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION receive FDA 510(k) clearance?

MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION received FDA 510(k) clearance on 1994-05-02, under 510(k) number K921370.

Who is the listed applicant for MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION?

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

What is the FDA product code for MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION?

The FDA product code for MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION is KNT.

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Other records listing Medical Innovations 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.

K945612MIC NASOGASTRIC-GASTROJEJUNAL FEEDING TUBEK940548MIC PERCUTANEOUS ENDOSCOPIC JEJUNAL FEEDING TUBEK943685MIC DISPOSABLE SNAREK926581MIC TRANSGASTRIC JEJUNAL TUBEK921652MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KITK924065MIC PEG 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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