VEN-O-VAC BLOOD COLLECTION VACUUM TUBES
K-Number: K900856 · 1990-09-21
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Device Summary
Frequently Asked Questions
What is the VEN-O-VAC BLOOD COLLECTION VACUUM TUBES?
VEN-O-VAC BLOOD COLLECTION VACUUM TUBES is a medical device that received FDA 510(k) clearance on 1990-09-21. The listed applicant is Artefactos DE Vidrio S.A. DE C.V.. The 510(k) number is K900856.
When did VEN-O-VAC BLOOD COLLECTION VACUUM TUBES receive FDA 510(k) clearance?
VEN-O-VAC BLOOD COLLECTION VACUUM TUBES received FDA 510(k) clearance on 1990-09-21, under 510(k) number K900856.
Who is the listed applicant for VEN-O-VAC BLOOD COLLECTION VACUUM TUBES?
The FDA 510(k) record lists Artefactos DE Vidrio S.A. DE C.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VEN-O-VAC BLOOD COLLECTION VACUUM TUBES?
The FDA product code for VEN-O-VAC BLOOD COLLECTION VACUUM TUBES is JKA.
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.
Related Devices (Code: JKA)
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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