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FDA 510(k)

LOW PROFILE GASTROSTOMY

K-Number: K872771 · 1987-10-09

ApplicantMicrovasive
Decision Date1987-10-09
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LOW PROFILE GASTROSTOMY is the device name listed in this FDA 510(k) record. The listed applicant is Microvasive. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K872771. 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 LOW PROFILE GASTROSTOMY?

LOW PROFILE GASTROSTOMY is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Microvasive. The 510(k) number is K872771.

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

LOW PROFILE GASTROSTOMY received FDA 510(k) clearance on 1987-10-09, under 510(k) number K872771.

Who is the listed applicant for LOW PROFILE GASTROSTOMY?

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

What is the FDA product code for LOW PROFILE GASTROSTOMY?

The FDA product code for LOW PROFILE GASTROSTOMY is KNT.

Related Clinical Trials

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.

Other records listing Microvasive as applicant

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.

View all 18 devices →

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.

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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