CATHETER, THERMAL DILUTION, ANIMAL & PED
K-Number: K760064 · 1976-07-21
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Device Summary
Frequently Asked Questions
What is the CATHETER, THERMAL DILUTION, ANIMAL & PED?
CATHETER, THERMAL DILUTION, ANIMAL & PED is a medical device that received FDA 510(k) clearance on 1976-07-21. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K760064.
When did CATHETER, THERMAL DILUTION, ANIMAL & PED receive FDA 510(k) clearance?
CATHETER, THERMAL DILUTION, ANIMAL & PED received FDA 510(k) clearance on 1976-07-21, under 510(k) number K760064.
Who is the listed applicant for CATHETER, THERMAL DILUTION, ANIMAL & PED?
The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATHETER, THERMAL DILUTION, ANIMAL & PED?
The FDA product code for CATHETER, THERMAL DILUTION, ANIMAL & PED is KRB.
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 Instrumentation Laboratory 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: KRB)
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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