TREATMENT TABLE
K-Number: K910838 · 1991-08-07
Advertisement
Device Summary
Frequently Asked Questions
What is the TREATMENT TABLE?
TREATMENT TABLE is a medical device that received FDA 510(k) clearance on 1991-08-07. The listed applicant is Tri W-G, Inc.. The 510(k) number is K910838.
When did TREATMENT TABLE receive FDA 510(k) clearance?
TREATMENT TABLE received FDA 510(k) clearance on 1991-08-07, under 510(k) number K910838.
Who is the listed applicant for TREATMENT TABLE?
The FDA 510(k) record lists Tri W-G, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TREATMENT TABLE?
The FDA product code for TREATMENT TABLE is IXR.
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 Tri W-G, 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: IXR)
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