VERI/PMS MODEL 815
K-Number: K810496 · 1981-03-13
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Device Summary
Frequently Asked Questions
What is the VERI/PMS MODEL 815?
VERI/PMS MODEL 815 is a medical device that received FDA 510(k) clearance on 1981-03-13. The listed applicant is Verite. The 510(k) number is K810496.
When did VERI/PMS MODEL 815 receive FDA 510(k) clearance?
VERI/PMS MODEL 815 received FDA 510(k) clearance on 1981-03-13, under 510(k) number K810496.
Who is the listed applicant for VERI/PMS MODEL 815?
The FDA 510(k) record lists Verite as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERI/PMS MODEL 815?
The FDA product code for VERI/PMS MODEL 815 is IPF.
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 Verite 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: IPF)
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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