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FDA 510(k)

SODIUM CITRATE

K-Number: K761177 · 1977-01-10

ApplicantBio/Data Corp.
Decision Date1977-01-10
Product CodeGJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SODIUM CITRATE is the device name listed in this FDA 510(k) record. The listed applicant is Bio/Data Corp.. It received FDA 510(k) clearance on 1977-01-10 under 510(k) number K761177. The device is classified under product code GJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SODIUM CITRATE?

SODIUM CITRATE is a medical device that received FDA 510(k) clearance on 1977-01-10. The listed applicant is Bio/Data Corp.. The 510(k) number is K761177.

When did SODIUM CITRATE receive FDA 510(k) clearance?

SODIUM CITRATE received FDA 510(k) clearance on 1977-01-10, under 510(k) number K761177.

Who is the listed applicant for SODIUM CITRATE?

The FDA 510(k) record lists Bio/Data Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SODIUM CITRATE?

The FDA product code for SODIUM CITRATE is GJE.

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Other records listing Bio/Data Corp. as applicant

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Related Devices (Code: GJE)

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.

K962596CUSTOMED BLOOD EXTRACTION KITCustomed, Inc.K925468JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KITJ.J. Skinner, Inc.K780303AUTO ISO-FILTER COLLECTION TUBE CAPBd Becton Dickinson Vacutainer Systems PreanalyticK771489RTERIAL BLOOD SAMPLING KITBd Becton Dickinson Vacutainer Systems PreanalyticK771370ICROTAINEO BRAND TUBEBd Becton Dickinson Vacutainer Systems PreanalyticK760086TRAY, BLOOD SAMPLING (PULSATOR II)Concord Laboratories, 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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