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FDA 510(k)

CORVAC PLASTIC BLOOD COLLECTION TUBE

K-Number: K944814 · 1994-12-19

ApplicantSherwood Medical Co.
Decision Date1994-12-19
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CORVAC PLASTIC 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 1994-12-19 under 510(k) number K944814. 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 PLASTIC BLOOD COLLECTION TUBE?

CORVAC PLASTIC BLOOD COLLECTION TUBE is a medical device that received FDA 510(k) clearance on 1994-12-19. The listed applicant is Sherwood Medical Co.. The 510(k) number is K944814.

When did CORVAC PLASTIC BLOOD COLLECTION TUBE receive FDA 510(k) clearance?

CORVAC PLASTIC BLOOD COLLECTION TUBE received FDA 510(k) clearance on 1994-12-19, under 510(k) number K944814.

Who is the listed applicant for CORVAC PLASTIC 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 PLASTIC BLOOD COLLECTION TUBE?

The FDA product code for CORVAC PLASTIC BLOOD COLLECTION TUBE is GIM.

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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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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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.

K240455BD Vacutainer® Citrate Blood Collection TubesBecton, Dickinson and CompanyK230493BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection TubeBecton, Dickinson and CompanyK213670BD Vacutainer K2EDTA Blood Collection Tubes, BD Vacutainer K3EDTA Blood Collection TubesBecton, Dickinson and CompanyK162723TransFix/EDTA Vacuum Blood Collection TubesCaltag Medsystems, Ltd.K080552CYTO-CHEX BCTStreckK012152DS30 HCY BLOOD COLLECTION TUBESDrew Scientific , Ltd.

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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