VERI/DFS TM #817
K-Number: K813515 · 1982-01-19
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Device Summary
Frequently Asked Questions
What is the VERI/DFS TM #817?
VERI/DFS TM #817 is a medical device that received FDA 510(k) clearance on 1982-01-19. The listed applicant is Verite. The 510(k) number is K813515.
When did VERI/DFS TM #817 receive FDA 510(k) clearance?
VERI/DFS TM #817 received FDA 510(k) clearance on 1982-01-19, under 510(k) number K813515.
Who is the listed applicant for VERI/DFS TM #817?
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/DFS TM #817?
The FDA product code for VERI/DFS TM #817 is GZI.
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: GZI)
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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