HI-LO TABLE, MODEL 820-05
K-Number: K882917 · 1988-07-28
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Device Summary
Frequently Asked Questions
What is the HI-LO TABLE, MODEL 820-05?
HI-LO TABLE, MODEL 820-05 is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Tri W-G, Inc.. The 510(k) number is K882917.
When did HI-LO TABLE, MODEL 820-05 receive FDA 510(k) clearance?
HI-LO TABLE, MODEL 820-05 received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882917.
Who is the listed applicant for HI-LO TABLE, MODEL 820-05?
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 HI-LO TABLE, MODEL 820-05?
The FDA product code for HI-LO TABLE, MODEL 820-05 is JFB.
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: JFB)
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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