COMPACT 2000
K-Number: K851892 · 1985-06-14
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Device Summary
Frequently Asked Questions
What is the COMPACT 2000?
COMPACT 2000 is a medical device that received FDA 510(k) clearance on 1985-06-14. The listed applicant is Atrium Medical Corp.. The 510(k) number is K851892.
When did COMPACT 2000 receive FDA 510(k) clearance?
COMPACT 2000 received FDA 510(k) clearance on 1985-06-14, under 510(k) number K851892.
Who is the listed applicant for COMPACT 2000?
The FDA 510(k) record lists Atrium Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMPACT 2000?
The FDA product code for COMPACT 2000 is KDQ.
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 Atrium Medical Corp. 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: KDQ)
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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