TOWEL CLIPS
K-Number: K890159 · 1989-02-03
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Device Summary
Frequently Asked Questions
What is the TOWEL CLIPS?
TOWEL CLIPS is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Dhason Brothers, Inc.. The 510(k) number is K890159.
When did TOWEL CLIPS receive FDA 510(k) clearance?
TOWEL CLIPS received FDA 510(k) clearance on 1989-02-03, under 510(k) number K890159.
Who is the listed applicant for TOWEL CLIPS?
The FDA 510(k) record lists Dhason Brothers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TOWEL CLIPS?
The FDA product code for TOWEL CLIPS is GDO.
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 Dhason Brothers, 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: GDO)
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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