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FDA 510(k)

SCEPTOR BETA-LACTAM PLUS MIC PANEL

K-Number: K844231 · 1984-11-07

Decision Date1984-11-07
Product CodeLTW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SCEPTOR BETA-LACTAM PLUS MIC PANEL 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 1984-11-07 under 510(k) number K844231. The device is classified under product code LTW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCEPTOR BETA-LACTAM PLUS MIC PANEL?

SCEPTOR BETA-LACTAM PLUS MIC PANEL is a medical device that received FDA 510(k) clearance on 1984-11-07. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K844231.

When did SCEPTOR BETA-LACTAM PLUS MIC PANEL receive FDA 510(k) clearance?

SCEPTOR BETA-LACTAM PLUS MIC PANEL received FDA 510(k) clearance on 1984-11-07, under 510(k) number K844231.

Who is the listed applicant for SCEPTOR BETA-LACTAM PLUS MIC PANEL?

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 BETA-LACTAM PLUS MIC PANEL?

The FDA product code for SCEPTOR BETA-LACTAM PLUS MIC PANEL is LTW.

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: LTW)

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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