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FDA 510(k)

CORVAC BLOOD COLLECTION TUBE

K-Number: K915213 · 1992-01-08

Decision Date1992-01-08
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CORVAC BLOOD COLLECTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1992-01-08 under 510(k) number K915213. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 191 devices →

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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