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FDA 510(k)

VEN-O-VAC BLOOD COLLECTION VACUUM TUBES

K-Number: K900856 · 1990-09-21

Decision Date1990-09-21
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VEN-O-VAC BLOOD COLLECTION VACUUM TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Artefactos DE Vidrio S.A. DE C.V.. It received FDA 510(k) clearance on 1990-09-21 under 510(k) number K900856. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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