CORVAC BLOOD COLLECTION TUBE
K-Number: K915213 · 1992-01-08
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Device Summary
Frequently Asked Questions
What is the CORVAC BLOOD COLLECTION TUBE?
CORVAC BLOOD COLLECTION TUBE is a medical device that received FDA 510(k) clearance on 1992-01-08. The listed applicant is Sherwood Medical Co.. The 510(k) number is K915213.
When did CORVAC BLOOD COLLECTION TUBE receive FDA 510(k) clearance?
CORVAC BLOOD COLLECTION TUBE received FDA 510(k) clearance on 1992-01-08, under 510(k) number K915213.
Who is the listed applicant for CORVAC BLOOD COLLECTION TUBE?
The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CORVAC BLOOD COLLECTION TUBE?
The FDA product code for CORVAC BLOOD COLLECTION TUBE is GIM.
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 Sherwood Medical Co. 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: GIM)
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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