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FDA 510(k)

DYNAMARK 1000

K-Number: K873979 · 1987-11-27

Decision Date1987-11-27
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DYNAMARK 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Dynamedics, Inc.. It received FDA 510(k) clearance on 1987-11-27 under 510(k) number K873979. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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