HOLLISTER VERTICAL DRAIN/TUBE ATTACHMENT DEVICE
K-Number: K932855 · 1993-10-13
Advertisement
Device Summary
Frequently Asked Questions
What is the HOLLISTER VERTICAL DRAIN/TUBE ATTACHMENT DEVICE?
HOLLISTER VERTICAL DRAIN/TUBE ATTACHMENT DEVICE is a medical device that received FDA 510(k) clearance on 1993-10-13. The listed applicant is Hollister, Inc.. The 510(k) number is K932855.
When did HOLLISTER VERTICAL DRAIN/TUBE ATTACHMENT DEVICE receive FDA 510(k) clearance?
HOLLISTER VERTICAL DRAIN/TUBE ATTACHMENT DEVICE received FDA 510(k) clearance on 1993-10-13, under 510(k) number K932855.
Who is the listed applicant for HOLLISTER VERTICAL DRAIN/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 VERTICAL DRAIN/TUBE ATTACHMENT DEVICE?
The FDA product code for HOLLISTER VERTICAL DRAIN/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.
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.
Advertisement