CHRONODYNAMICS DATA RECORDER (CDR)-100
K-Number: K881813 · 1988-12-05
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Device Summary
Frequently Asked Questions
What is the CHRONODYNAMICS DATA RECORDER (CDR)-100?
CHRONODYNAMICS DATA RECORDER (CDR)-100 is a medical device that received FDA 510(k) clearance on 1988-12-05. The listed applicant is Chronodynamics, Inc.. The 510(k) number is K881813.
When did CHRONODYNAMICS DATA RECORDER (CDR)-100 receive FDA 510(k) clearance?
CHRONODYNAMICS DATA RECORDER (CDR)-100 received FDA 510(k) clearance on 1988-12-05, under 510(k) number K881813.
Who is the listed applicant for CHRONODYNAMICS DATA RECORDER (CDR)-100?
The FDA 510(k) record lists Chronodynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHRONODYNAMICS DATA RECORDER (CDR)-100?
The FDA product code for CHRONODYNAMICS DATA RECORDER (CDR)-100 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.
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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