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FDA 510(k)

FLEXIFLO OVER-THE-GUIDEWIRE GASTROSTOMY KIT

K-Number: K915110 · 1992-04-14

ApplicantAbbott Laboratories
Decision Date1992-04-14
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

FLEXIFLO OVER-THE-GUIDEWIRE GASTROSTOMY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1992-04-14 under 510(k) number K915110. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the FLEXIFLO OVER-THE-GUIDEWIRE GASTROSTOMY KIT?

FLEXIFLO OVER-THE-GUIDEWIRE GASTROSTOMY KIT is a medical device that received FDA 510(k) clearance on 1992-04-14. The listed applicant is Abbott Laboratories. The 510(k) number is K915110.

When did FLEXIFLO OVER-THE-GUIDEWIRE GASTROSTOMY KIT receive FDA 510(k) clearance?

FLEXIFLO OVER-THE-GUIDEWIRE GASTROSTOMY KIT received FDA 510(k) clearance on 1992-04-14, under 510(k) number K915110.

Who is the listed applicant for FLEXIFLO OVER-THE-GUIDEWIRE GASTROSTOMY KIT?

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 OVER-THE-GUIDEWIRE GASTROSTOMY KIT?

The FDA product code for FLEXIFLO OVER-THE-GUIDEWIRE GASTROSTOMY KIT is KNT.

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Related Devices (Code: KNT)

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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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