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FDA 510(k)

HI-LO TABLE, MODEL 820-05

K-Number: K882917 · 1988-07-28

ApplicantTri W-G, Inc.
Decision Date1988-07-28
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HI-LO TABLE, MODEL 820-05 is the device name listed in this FDA 510(k) record. The listed applicant is Tri W-G, Inc.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K882917. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 35 devices →

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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