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FDA 510(k)

SCEPTOR ID GRAM NEGATIVE MIC/ID PANELS

K-Number: K811434 · 1981-06-26

Decision Date1981-06-26
Product CodeJSS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SCEPTOR ID GRAM NEGATIVE MIC/ID PANELS 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 1981-06-26 under 510(k) number K811434. The device is classified under product code JSS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCEPTOR ID GRAM NEGATIVE MIC/ID PANELS?

SCEPTOR ID GRAM NEGATIVE MIC/ID PANELS is a medical device that received FDA 510(k) clearance on 1981-06-26. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K811434.

When did SCEPTOR ID GRAM NEGATIVE MIC/ID PANELS receive FDA 510(k) clearance?

SCEPTOR ID GRAM NEGATIVE MIC/ID PANELS received FDA 510(k) clearance on 1981-06-26, under 510(k) number K811434.

Who is the listed applicant for SCEPTOR ID GRAM NEGATIVE MIC/ID PANELS?

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 SCEPTOR ID GRAM NEGATIVE MIC/ID PANELS?

The FDA product code for SCEPTOR ID GRAM NEGATIVE MIC/ID PANELS is JSS.

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: JSS)

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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