910T MONTORIZED INSTRUMENT TABLE
K-Number: K922242 · 1992-09-30
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Device Summary
Frequently Asked Questions
What is the 910T MONTORIZED INSTRUMENT TABLE?
910T MONTORIZED INSTRUMENT TABLE is a medical device that received FDA 510(k) clearance on 1992-09-30. The listed applicant is R.H. Burton Co.. The 510(k) number is K922242.
When did 910T MONTORIZED INSTRUMENT TABLE receive FDA 510(k) clearance?
910T MONTORIZED INSTRUMENT TABLE received FDA 510(k) clearance on 1992-09-30, under 510(k) number K922242.
Who is the listed applicant for 910T MONTORIZED INSTRUMENT TABLE?
The FDA 510(k) record lists R.H. Burton Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 910T MONTORIZED INSTRUMENT TABLE?
The FDA product code for 910T MONTORIZED INSTRUMENT TABLE is HRJ.
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 R.H. Burton Co. 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: HRJ)
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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