CT-1000A SYSTEM
K-Number: K896779 · 1990-06-01
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Device Summary
Frequently Asked Questions
What is the CT-1000A SYSTEM?
CT-1000A SYSTEM is a medical device that received FDA 510(k) clearance on 1990-06-01. The listed applicant is Bio-Monitor, Inc.. The 510(k) number is K896779.
When did CT-1000A SYSTEM receive FDA 510(k) clearance?
CT-1000A SYSTEM received FDA 510(k) clearance on 1990-06-01, under 510(k) number K896779.
Who is the listed applicant for CT-1000A SYSTEM?
The FDA 510(k) record lists Bio-Monitor, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CT-1000A SYSTEM?
The FDA product code for CT-1000A SYSTEM 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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