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FDA 510(k)

LOW PROFILE GASTROMSTOMY DEVICE

K-Number: K923474 · 1993-01-05

ApplicantBiosearch Medical Products, Inc.
Decision Date1993-01-05
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

LOW PROFILE GASTROMSTOMY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Biosearch Medical Products, Inc.. It received FDA 510(k) clearance on 1993-01-05 under 510(k) number K923474. 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 LOW PROFILE GASTROMSTOMY DEVICE?

LOW PROFILE GASTROMSTOMY DEVICE is a medical device that received FDA 510(k) clearance on 1993-01-05. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K923474.

When did LOW PROFILE GASTROMSTOMY DEVICE receive FDA 510(k) clearance?

LOW PROFILE GASTROMSTOMY DEVICE received FDA 510(k) clearance on 1993-01-05, under 510(k) number K923474.

Who is the listed applicant for LOW PROFILE GASTROMSTOMY DEVICE?

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

What is the FDA product code for LOW PROFILE GASTROMSTOMY DEVICE?

The FDA product code for LOW PROFILE GASTROMSTOMY DEVICE is KNT.

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Other records listing Biosearch Medical Products, Inc. as applicant

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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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