MODIFIED SEISMOCARDIOGRAPH
K-Number: K900130 · 1990-03-28
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Device Summary
Frequently Asked Questions
What is the MODIFIED SEISMOCARDIOGRAPH?
MODIFIED SEISMOCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 1990-03-28. The listed applicant is Seismed Instruments, Inc.. The 510(k) number is K900130.
When did MODIFIED SEISMOCARDIOGRAPH receive FDA 510(k) clearance?
MODIFIED SEISMOCARDIOGRAPH received FDA 510(k) clearance on 1990-03-28, under 510(k) number K900130.
Who is the listed applicant for MODIFIED SEISMOCARDIOGRAPH?
The FDA 510(k) record lists Seismed Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED SEISMOCARDIOGRAPH?
The FDA product code for MODIFIED SEISMOCARDIOGRAPH is DSB.
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 Seismed Instruments, 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: DSB)
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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