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FDA 510(k)

NASOGASTRIC FEEDING TUBE KITS

K-Number: K915439 · 1992-02-25

Decision Date1992-02-25
Product CodeFPD
Advisory CommitteeGU
DecisionUnknown

Device Summary

NASOGASTRIC FEEDING TUBE KITS is the device name listed in this FDA 510(k) record. The listed applicant is Sandoz Nutrition. It received FDA 510(k) clearance on 1992-02-25 under 510(k) number K915439. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NASOGASTRIC FEEDING TUBE KITS?

NASOGASTRIC FEEDING TUBE KITS is a medical device that received FDA 510(k) clearance on 1992-02-25. The listed applicant is Sandoz Nutrition. The 510(k) number is K915439.

When did NASOGASTRIC FEEDING TUBE KITS receive FDA 510(k) clearance?

NASOGASTRIC FEEDING TUBE KITS received FDA 510(k) clearance on 1992-02-25, under 510(k) number K915439.

Who is the listed applicant for NASOGASTRIC FEEDING TUBE KITS?

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

What is the FDA product code for NASOGASTRIC FEEDING TUBE KITS?

The FDA product code for NASOGASTRIC FEEDING TUBE KITS 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 Sandoz Nutrition 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.

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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

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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