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FDA 510(k)

BACTEC DILUTING FLUID

K-Number: K822330 · 1982-09-02

Decision Date1982-09-02
Product CodeJSD
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BACTEC DILUTING FLUID 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 1982-09-02 under 510(k) number K822330. The device is classified under product code JSD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACTEC DILUTING FLUID?

BACTEC DILUTING FLUID is a medical device that received FDA 510(k) clearance on 1982-09-02. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K822330.

When did BACTEC DILUTING FLUID receive FDA 510(k) clearance?

BACTEC DILUTING FLUID received FDA 510(k) clearance on 1982-09-02, under 510(k) number K822330.

Who is the listed applicant for BACTEC DILUTING FLUID?

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 BACTEC DILUTING FLUID?

The FDA product code for BACTEC DILUTING FLUID is JSD.

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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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 632 devices →

Related Devices (Code: JSD)

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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