VES-TEC/VES-MATIC
K-Number: K854223 · 1986-04-04
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Device Summary
Frequently Asked Questions
What is the VES-TEC/VES-MATIC?
VES-TEC/VES-MATIC is a medical device that received FDA 510(k) clearance on 1986-04-04. The listed applicant is Marvic Interpharma, Inc.. The 510(k) number is K854223.
When did VES-TEC/VES-MATIC receive FDA 510(k) clearance?
VES-TEC/VES-MATIC received FDA 510(k) clearance on 1986-04-04, under 510(k) number K854223.
Who is the listed applicant for VES-TEC/VES-MATIC?
The FDA 510(k) record lists Marvic Interpharma, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VES-TEC/VES-MATIC?
The FDA product code for VES-TEC/VES-MATIC is CKB.
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 Marvic Interpharma, 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: CKB)
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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