MYOCARDIAL TEMPERATURE MONITORING PROBES, CJ-1000
K-Number: K905652 · 1991-02-14
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Device Summary
Frequently Asked Questions
What is the MYOCARDIAL TEMPERATURE MONITORING PROBES, CJ-1000?
MYOCARDIAL TEMPERATURE MONITORING PROBES, CJ-1000 is a medical device that received FDA 510(k) clearance on 1991-02-14. The listed applicant is Daily Medical Products, Inc.. The 510(k) number is K905652.
When did MYOCARDIAL TEMPERATURE MONITORING PROBES, CJ-1000 receive FDA 510(k) clearance?
MYOCARDIAL TEMPERATURE MONITORING PROBES, CJ-1000 received FDA 510(k) clearance on 1991-02-14, under 510(k) number K905652.
Who is the listed applicant for MYOCARDIAL TEMPERATURE MONITORING PROBES, CJ-1000?
The FDA 510(k) record lists Daily Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MYOCARDIAL TEMPERATURE MONITORING PROBES, CJ-1000?
The FDA product code for MYOCARDIAL TEMPERATURE MONITORING PROBES, CJ-1000 is FLL.
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 Daily Medical Products, 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: FLL)
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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