TABLE, MODELS 610,611 & 612
K-Number: K834103 · 1984-01-13
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Device Summary
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.
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
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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