CARDIOZYME CK CONTROL NORMAL
K-Number: K770973 · 1977-08-04
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Device Summary
Frequently Asked Questions
What is the CARDIOZYME CK CONTROL NORMAL?
CARDIOZYME CK CONTROL NORMAL is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. The 510(k) number is K770973.
When did CARDIOZYME CK CONTROL NORMAL receive FDA 510(k) clearance?
CARDIOZYME CK CONTROL NORMAL received FDA 510(k) clearance on 1977-08-04, under 510(k) number K770973.
Who is the listed applicant for CARDIOZYME CK CONTROL NORMAL?
The FDA 510(k) record lists Dade, Baxter Travenol Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARDIOZYME CK CONTROL NORMAL?
The FDA product code for CARDIOZYME CK CONTROL NORMAL is JJT.
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 Dade, Baxter Travenol Diagnostics, 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: JJT)
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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