DINAMAP MODEL 855
K-Number: K791159 · 1979-07-30
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Device Summary
Frequently Asked Questions
What is the DINAMAP MODEL 855?
DINAMAP MODEL 855 is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Applied Medical Research. The 510(k) number is K791159.
When did DINAMAP MODEL 855 receive FDA 510(k) clearance?
DINAMAP MODEL 855 received FDA 510(k) clearance on 1979-07-30, under 510(k) number K791159.
Who is the listed applicant for DINAMAP MODEL 855?
The FDA 510(k) record lists Applied Medical Research as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DINAMAP MODEL 855?
The FDA product code for DINAMAP MODEL 855 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 Applied Medical Research 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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