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FDA 510(k)

TUBE GASTROSTOMY

K-Number: K903086 · 1990-11-20

ApplicantKnight Medical, Inc.
Decision Date1990-11-20
Product CodeKGC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TUBE GASTROSTOMY is the device name listed in this FDA 510(k) record. The listed applicant is Knight Medical, Inc.. It received FDA 510(k) clearance on 1990-11-20 under 510(k) number K903086. The device is classified under product code KGC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBE GASTROSTOMY?

TUBE GASTROSTOMY is a medical device that received FDA 510(k) clearance on 1990-11-20. The listed applicant is Knight Medical, Inc.. The 510(k) number is K903086.

When did TUBE GASTROSTOMY receive FDA 510(k) clearance?

TUBE GASTROSTOMY received FDA 510(k) clearance on 1990-11-20, under 510(k) number K903086.

Who is the listed applicant for TUBE GASTROSTOMY?

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

What is the FDA product code for TUBE GASTROSTOMY?

The FDA product code for TUBE GASTROSTOMY is KGC.

Related Clinical Trials

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.

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Other records listing Knight Medical, 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.

K921127PANDA NEEDLE CATHETER JEJUNOSTOMY KITK883848KMI OXY-BANK883886DOUBLE CLOSED URINARY DRAINAGE SYSTEMK862489ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE

Related Devices (Code: KGC)

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.

K242211PUMA-G Pediatric SystemCoaptech, Inc.K223916PUMA-G SystemCoaptech, Inc.K193612AMT Suture Delivery SystemApplied Medical Technology, Inc.K191844Fidmi Low Profile Enteral Feeding DeviceFidmi Medical, Ltd.K182832Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor SetCook IncorporatedK183057PUMA-G SystemCoaptech, 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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