RT-200 CALIBRATION ANALYZER
K-Number: K822746 · 1982-10-13
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Device Summary
Frequently Asked Questions
What is the RT-200 CALIBRATION ANALYZER?
RT-200 CALIBRATION ANALYZER is a medical device that received FDA 510(k) clearance on 1982-10-13. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K822746.
When did RT-200 CALIBRATION ANALYZER receive FDA 510(k) clearance?
RT-200 CALIBRATION ANALYZER received FDA 510(k) clearance on 1982-10-13, under 510(k) number K822746.
Who is the listed applicant for RT-200 CALIBRATION ANALYZER?
The FDA 510(k) record lists Timeter Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RT-200 CALIBRATION ANALYZER?
The FDA product code for RT-200 CALIBRATION ANALYZER is BXX.
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 Timeter Instrument Corp. 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: BXX)
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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