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FDA 510(k)

KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE

K-Number: K880850 · 1988-05-26

ApplicantKmb Medical Products Co.
Decision Date1988-05-26
Product CodeFEG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Kmb Medical Products Co.. It received FDA 510(k) clearance on 1988-05-26 under 510(k) number K880850. The device is classified under product code FEG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE?

KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE is a medical device that received FDA 510(k) clearance on 1988-05-26. The listed applicant is Kmb Medical Products Co.. The 510(k) number is K880850.

When did KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE receive FDA 510(k) clearance?

KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE received FDA 510(k) clearance on 1988-05-26, under 510(k) number K880850.

Who is the listed applicant for KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE?

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

What is the FDA product code for KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE?

The FDA product code for KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE is FEG.

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Related Devices (Code: FEG)

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.

K17161914Fr Colon Decompression Set, Macon Colon Decompression SetCook Ireland, Ltd.K132314MEDLINE ANTI-REFLUX VALVEMedline Industries, Inc.K053410GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTORKendallK040388NEXT GENERATION SALEM SUMPKendallK971354KNOTT NG TUBEMichael M. Knott, M.D.K960176DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTERC.R. Bard, Inc.

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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