FDA 510(k)

NH PEDIATRIC REPLACEMENT GASTROSTOMY KIT

K-Number: K884309 · 1988-12-08

ApplicantBiosearch Medical Products, Inc.

Decision Date1988-12-08

Product CodeKNT

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

NH PEDIATRIC REPLACEMENT GASTROSTOMY KIT 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 1988-12-08 under 510(k) number K884309. 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 NH PEDIATRIC REPLACEMENT GASTROSTOMY KIT?

NH PEDIATRIC REPLACEMENT GASTROSTOMY KIT is a medical device that received FDA 510(k) clearance on 1988-12-08. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K884309.

When did NH PEDIATRIC REPLACEMENT GASTROSTOMY KIT receive FDA 510(k) clearance?

NH PEDIATRIC REPLACEMENT GASTROSTOMY KIT received FDA 510(k) clearance on 1988-12-08, under 510(k) number K884309.

Who is the listed applicant for NH PEDIATRIC REPLACEMENT GASTROSTOMY KIT?

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 NH PEDIATRIC REPLACEMENT GASTROSTOMY KIT?

The FDA product code for NH PEDIATRIC REPLACEMENT GASTROSTOMY KIT is KNT.

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Other records listing Biosearch Medical Products, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.