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FDA 510(k)

TABLE, MODELS 610,611 & 612

K-Number: K834103 · 1984-01-13

ApplicantTri W-G, Inc.
Decision Date1984-01-13
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TABLE, MODELS 610,611 & 612 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 1984-01-13 under 510(k) number K834103. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TABLE, MODELS 610,611 & 612?

TABLE, MODELS 610,611 & 612 is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Tri W-G, Inc.. The 510(k) number is K834103.

When did TABLE, MODELS 610,611 & 612 receive FDA 510(k) clearance?

TABLE, MODELS 610,611 & 612 received FDA 510(k) clearance on 1984-01-13, under 510(k) number K834103.

Who is the listed applicant for TABLE, MODELS 610,611 & 612?

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 TABLE, MODELS 610,611 & 612?

The FDA product code for TABLE, MODELS 610,611 & 612 is INQ.

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.

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Related Devices (Code: INQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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