DYNAMARK 1000
K-Number: K873979 · 1987-11-27
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Device Summary
Frequently Asked Questions
What is the DYNAMARK 1000?
DYNAMARK 1000 is a medical device that received FDA 510(k) clearance on 1987-11-27. The listed applicant is Dynamedics, Inc.. The 510(k) number is K873979.
When did DYNAMARK 1000 receive FDA 510(k) clearance?
DYNAMARK 1000 received FDA 510(k) clearance on 1987-11-27, under 510(k) number K873979.
Who is the listed applicant for DYNAMARK 1000?
The FDA 510(k) record lists Dynamedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNAMARK 1000?
The FDA product code for DYNAMARK 1000 is DXN.
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 Dynamedics, 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: DXN)
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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