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FDA 510(k)

JEJENOSTOMY FEEDING TUBE

K-Number: K971906 · 1997-08-20

Decision Date1997-08-20
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

JEJENOSTOMY FEEDING TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1997-08-20 under 510(k) number K971906. 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 JEJENOSTOMY FEEDING TUBE?

JEJENOSTOMY FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1997-08-20. The listed applicant is Boston Scientific Corp. The 510(k) number is K971906.

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

JEJENOSTOMY FEEDING TUBE received FDA 510(k) clearance on 1997-08-20, under 510(k) number K971906.

Who is the listed applicant for JEJENOSTOMY FEEDING TUBE?

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

What is the FDA product code for JEJENOSTOMY FEEDING TUBE?

The FDA product code for JEJENOSTOMY FEEDING TUBE 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 Boston Scientific 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.

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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

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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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