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FDA 510(k)

NOVARTIS COMPAT SURGICAL GASTROSTOMY JEJUNOSTOMY FEEDING TUBE KIT

K-Number: K071191 · 2007-07-23

Decision Date2007-07-23
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NOVARTIS COMPAT SURGICAL GASTROSTOMY JEJUNOSTOMY FEEDING TUBE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Novartis Nutrition Corp.. It received FDA 510(k) clearance on 2007-07-23 under 510(k) number K071191. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVARTIS COMPAT SURGICAL GASTROSTOMY JEJUNOSTOMY FEEDING TUBE KIT?

NOVARTIS COMPAT SURGICAL GASTROSTOMY JEJUNOSTOMY FEEDING TUBE KIT is a medical device that received FDA 510(k) clearance on 2007-07-23. The listed applicant is Novartis Nutrition Corp.. The 510(k) number is K071191.

When did NOVARTIS COMPAT SURGICAL GASTROSTOMY JEJUNOSTOMY FEEDING TUBE KIT receive FDA 510(k) clearance?

NOVARTIS COMPAT SURGICAL GASTROSTOMY JEJUNOSTOMY FEEDING TUBE KIT received FDA 510(k) clearance on 2007-07-23, under 510(k) number K071191.

Who is the listed applicant for NOVARTIS COMPAT SURGICAL GASTROSTOMY JEJUNOSTOMY FEEDING TUBE KIT?

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

What is the FDA product code for NOVARTIS COMPAT SURGICAL GASTROSTOMY JEJUNOSTOMY FEEDING TUBE KIT?

The FDA product code for NOVARTIS COMPAT SURGICAL GASTROSTOMY JEJUNOSTOMY FEEDING TUBE KIT is FPD.

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.

Other records listing Novartis Nutrition 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.

Related Devices (Code: FPD)

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.

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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