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FDA 510(k)

REGU-VAC OXYGENATING SUCTION CATHETER

K-Number: K813220 · 1982-01-22

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1982-01-22
Product Code
DecisionSubstantially Equivalent

Device Summary

REGU-VAC OXYGENATING SUCTION CATHETER 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 1982-01-22 under 510(k) number K813220. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REGU-VAC OXYGENATING SUCTION CATHETER?

REGU-VAC OXYGENATING SUCTION CATHETER is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K813220.

When did REGU-VAC OXYGENATING SUCTION CATHETER receive FDA 510(k) clearance?

REGU-VAC OXYGENATING SUCTION CATHETER received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813220.

Who is the listed applicant for REGU-VAC OXYGENATING SUCTION CATHETER?

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

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.

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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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