ROCHE COBAS(R) AMMONIA AND ETHANOL CALIBRATOR
K-Number: K914750 · 1991-11-22
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Device Summary
Frequently Asked Questions
What is the ROCHE COBAS(R) AMMONIA AND ETHANOL CALIBRATOR?
ROCHE COBAS(R) AMMONIA AND ETHANOL CALIBRATOR is a medical device that received FDA 510(k) clearance on 1991-11-22. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K914750.
When did ROCHE COBAS(R) AMMONIA AND ETHANOL CALIBRATOR receive FDA 510(k) clearance?
ROCHE COBAS(R) AMMONIA AND ETHANOL CALIBRATOR received FDA 510(k) clearance on 1991-11-22, under 510(k) number K914750.
Who is the listed applicant for ROCHE COBAS(R) AMMONIA AND ETHANOL CALIBRATOR?
The FDA 510(k) record lists Roche Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROCHE COBAS(R) AMMONIA AND ETHANOL CALIBRATOR?
The FDA product code for ROCHE COBAS(R) AMMONIA AND ETHANOL CALIBRATOR is JIX.
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 Roche Diagnostic Systems, 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: JIX)
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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