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FDA 510(k)

CEFOPERAZONE 75MCG SENSI-DISC

K-Number: K821264 · 1982-06-22

Decision Date1982-06-22
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CEFOPERAZONE 75MCG SENSI-DISC 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 1982-06-22 under 510(k) number K821264. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEFOPERAZONE 75MCG SENSI-DISC?

CEFOPERAZONE 75MCG SENSI-DISC is a medical device that received FDA 510(k) clearance on 1982-06-22. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K821264.

When did CEFOPERAZONE 75MCG SENSI-DISC receive FDA 510(k) clearance?

CEFOPERAZONE 75MCG SENSI-DISC received FDA 510(k) clearance on 1982-06-22, under 510(k) number K821264.

Who is the listed applicant for CEFOPERAZONE 75MCG SENSI-DISC?

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 CEFOPERAZONE 75MCG SENSI-DISC?

The FDA product code for CEFOPERAZONE 75MCG SENSI-DISC is JTN.

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: JTN)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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