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FDA 510(k)

DISPOSABLE/BOROSILICATE CULTURE TUBES

K-Number: K760583 · 1976-10-03

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1976-10-03
Product Code
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE/BOROSILICATE CULTURE TUBES 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 1976-10-03 under 510(k) number K760583. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE/BOROSILICATE CULTURE TUBES?

DISPOSABLE/BOROSILICATE CULTURE TUBES is a medical device that received FDA 510(k) clearance on 1976-10-03. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K760583.

When did DISPOSABLE/BOROSILICATE CULTURE TUBES receive FDA 510(k) clearance?

DISPOSABLE/BOROSILICATE CULTURE TUBES received FDA 510(k) clearance on 1976-10-03, under 510(k) number K760583.

Who is the listed applicant for DISPOSABLE/BOROSILICATE CULTURE TUBES?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic as applicant

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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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