Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HOLLISTER FEEDING TUBE ATTACHMENT DEVICE

K-Number: K893888 · 1989-10-17

Decision Date1989-10-17
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOLLISTER FEEDING TUBE ATTACHMENT DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1989-10-17 under 510(k) number K893888. 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 HOLLISTER FEEDING TUBE ATTACHMENT DEVICE?

HOLLISTER FEEDING TUBE ATTACHMENT DEVICE is a medical device that received FDA 510(k) clearance on 1989-10-17. The listed applicant is Hollister, Inc.. The 510(k) number is K893888.

When did HOLLISTER FEEDING TUBE ATTACHMENT DEVICE receive FDA 510(k) clearance?

HOLLISTER FEEDING TUBE ATTACHMENT DEVICE received FDA 510(k) clearance on 1989-10-17, under 510(k) number K893888.

Who is the listed applicant for HOLLISTER FEEDING TUBE ATTACHMENT DEVICE?

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

What is the FDA product code for HOLLISTER FEEDING TUBE ATTACHMENT DEVICE?

The FDA product code for HOLLISTER FEEDING TUBE ATTACHMENT DEVICE 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 Hollister, Inc. 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 85 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.

↑