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FDA 510(k)

LEUCOPREP BRAND TUBE

K-Number: K872775 · 1987-10-02

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1987-10-02
Product CodeJCF
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LEUCOPREP BRAND TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1987-10-02 under 510(k) number K872775. The device is classified under product code JCF. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEUCOPREP BRAND TUBE?

LEUCOPREP BRAND TUBE is a medical device that received FDA 510(k) clearance on 1987-10-02. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K872775.

When did LEUCOPREP BRAND TUBE receive FDA 510(k) clearance?

LEUCOPREP BRAND TUBE received FDA 510(k) clearance on 1987-10-02, under 510(k) number K872775.

Who is the listed applicant for LEUCOPREP BRAND TUBE?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEUCOPREP BRAND TUBE?

The FDA product code for LEUCOPREP BRAND TUBE is JCF.

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Related Devices (Code: JCF)

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.

K911731LEUCOPREP(R) BRAND CELL SEPARAT TUBE W/SODIUM CITRBd Becton Dickinson Vacutainer Systems PreanalyticK902445LYMPHO SEP(TM)Icn Biomedicals, Inc.K891407LEUCOPREP CELL SEPARATION TUBEBd Becton Dickinson Vacutainer Systems PreanalyticK874328L-PHENYLALANINE METHYL ESTER HYDROCHLORIDE PME REAE.I. Dupont DE Nemours & Co., Inc.K873185DYNABEADS HLA CELL PREP II ISOLATION PRODUCTDynal Biotech, Inc.K860354SEPRACELL LYMPHOCYTE SEPARATION MEDIUMSepratech Corporation C/O Keller and Heckman

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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