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FDA 510(k)

VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE

K-Number: K873647 · 1987-10-20

ApplicantVentrex Laboratories, Inc.
Decision Date1987-10-20
Product CodeGIO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Ventrex Laboratories, Inc.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K873647. The device is classified under product code GIO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE?

VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K873647.

When did VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE receive FDA 510(k) clearance?

VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE received FDA 510(k) clearance on 1987-10-20, under 510(k) number K873647.

Who is the listed applicant for VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE?

The FDA 510(k) record lists Ventrex Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE?

The FDA product code for VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE is GIO.

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Other records listing Ventrex Laboratories, Inc. 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.

K914554SPECIFIC IGE EIA-TURBO ASSAYK913833VENTREX ALLERGEN DISCK913434VENTREX COATED TUBE INTACT PTHK905612VENTREX COATED TUBE IGE RADIOIMMUNOASSAYK905636VENTREX COATED TUBE IGE ENZYME IMMUNOASSAYK905247SHBG IRMA KIT

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Related Devices (Code: GIO)

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.

K972969QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEMInnovative Medical Technologies, Inc.K941291MONOJECT SAMPLETTE SEPARATOR TUBESherwood Medical Co.K894851TRU-TRAXHumagen, Inc.K885324HEMA(PRO)TEC(TION)Medical Products Search, Inc.K885138CAPILLARY TUBE, BLOOD COLLECTIONCoeur Laboratories, Inc.K884623SAFE-TEC CAPILLARY BLOOD COLLECTION TUBESafe-Tec Clinical Products, Inc.

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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