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FDA 510(k)

DURASAFE B-D COMBINED SPINAL EPIDURAL ANESTHESIA

K-Number: K932249 · 1993-08-27

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1993-08-27
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

DURASAFE B-D COMBINED SPINAL EPIDURAL ANESTHESIA 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 1993-08-27 under 510(k) number K932249. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DURASAFE B-D COMBINED SPINAL EPIDURAL ANESTHESIA?

DURASAFE B-D COMBINED SPINAL EPIDURAL ANESTHESIA is a medical device that received FDA 510(k) clearance on 1993-08-27. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K932249.

When did DURASAFE B-D COMBINED SPINAL EPIDURAL ANESTHESIA receive FDA 510(k) clearance?

DURASAFE B-D COMBINED SPINAL EPIDURAL ANESTHESIA received FDA 510(k) clearance on 1993-08-27, under 510(k) number K932249.

Who is the listed applicant for DURASAFE B-D COMBINED SPINAL EPIDURAL ANESTHESIA?

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 DURASAFE B-D COMBINED SPINAL EPIDURAL ANESTHESIA?

The FDA product code for DURASAFE B-D COMBINED SPINAL EPIDURAL ANESTHESIA is CAZ.

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Related Devices (Code: CAZ)

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Official Source

View on FDA Database →

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

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