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FDA 510(k)

FLEXIFLO LAPAROSCOPIC GASTROSTOMY KIT

K-Number: K924697 · 1993-08-27

ApplicantAbbott Laboratories
Decision Date1993-08-27
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

FLEXIFLO LAPAROSCOPIC 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 1993-08-27 under 510(k) number K924697. 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 LAPAROSCOPIC GASTROSTOMY KIT?

FLEXIFLO LAPAROSCOPIC GASTROSTOMY KIT is a medical device that received FDA 510(k) clearance on 1993-08-27. The listed applicant is Abbott Laboratories. The 510(k) number is K924697.

When did FLEXIFLO LAPAROSCOPIC GASTROSTOMY KIT receive FDA 510(k) clearance?

FLEXIFLO LAPAROSCOPIC GASTROSTOMY KIT received FDA 510(k) clearance on 1993-08-27, under 510(k) number K924697.

Who is the listed applicant for FLEXIFLO LAPAROSCOPIC 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 LAPAROSCOPIC GASTROSTOMY KIT?

The FDA product code for FLEXIFLO LAPAROSCOPIC 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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