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FDA 510(k)

FLEXIFLO TOPTAINER TOP-FILL ENTERAL NUTRIT. SYSTEM

K-Number: K871846 · 1987-08-26

ApplicantAbbott Laboratories
Decision Date1987-08-26
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEXIFLO TOPTAINER TOP-FILL ENTERAL NUTRIT. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1987-08-26 under 510(k) number K871846. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIFLO TOPTAINER TOP-FILL ENTERAL NUTRIT. SYSTEM?

FLEXIFLO TOPTAINER TOP-FILL ENTERAL NUTRIT. SYSTEM is a medical device that received FDA 510(k) clearance on 1987-08-26. The listed applicant is Abbott Laboratories. The 510(k) number is K871846.

When did FLEXIFLO TOPTAINER TOP-FILL ENTERAL NUTRIT. SYSTEM receive FDA 510(k) clearance?

FLEXIFLO TOPTAINER TOP-FILL ENTERAL NUTRIT. SYSTEM received FDA 510(k) clearance on 1987-08-26, under 510(k) number K871846.

Who is the listed applicant for FLEXIFLO TOPTAINER TOP-FILL ENTERAL NUTRIT. SYSTEM?

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

What is the FDA product code for FLEXIFLO TOPTAINER TOP-FILL ENTERAL NUTRIT. SYSTEM?

The FDA product code for FLEXIFLO TOPTAINER TOP-FILL ENTERAL NUTRIT. SYSTEM is KNT.

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Related Devices (Code: KNT)

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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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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