NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS
K-Number: K905248 · 1991-02-28
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Device Summary
Frequently Asked Questions
What is the NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS?
NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS is a medical device that received FDA 510(k) clearance on 1991-02-28. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K905248.
When did NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS receive FDA 510(k) clearance?
NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS received FDA 510(k) clearance on 1991-02-28, under 510(k) number K905248.
Who is the listed applicant for NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS?
The FDA 510(k) record lists Advanced Technology Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS?
The FDA product code for NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS is DQK.
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 Advanced Technology Laboratories, 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: DQK)
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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