DYNAMIC SPECTRAL PHONOCARDIOGRAPH
K-Number: K902185 · 1991-03-25
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Device Summary
Frequently Asked Questions
What is the DYNAMIC SPECTRAL PHONOCARDIOGRAPH?
DYNAMIC SPECTRAL PHONOCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 1991-03-25. The listed applicant is Reeves Scientific, Inc.. The 510(k) number is K902185.
When did DYNAMIC SPECTRAL PHONOCARDIOGRAPH receive FDA 510(k) clearance?
DYNAMIC SPECTRAL PHONOCARDIOGRAPH received FDA 510(k) clearance on 1991-03-25, under 510(k) number K902185.
Who is the listed applicant for DYNAMIC SPECTRAL PHONOCARDIOGRAPH?
The FDA 510(k) record lists Reeves Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNAMIC SPECTRAL PHONOCARDIOGRAPH?
The FDA product code for DYNAMIC SPECTRAL PHONOCARDIOGRAPH is DQC.
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: DQC)
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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