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FDA 510(k)

PUDENDAL/LOCAL ANESTESIA BLOCK TRAY

K-Number: K880988 · 1988-06-01

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1988-06-01
Product CodeKNE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PUDENDAL/LOCAL ANESTESIA BLOCK TRAY 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 1988-06-01 under 510(k) number K880988. The device is classified under product code KNE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PUDENDAL/LOCAL ANESTESIA BLOCK TRAY?

PUDENDAL/LOCAL ANESTESIA BLOCK TRAY is a medical device that received FDA 510(k) clearance on 1988-06-01. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K880988.

When did PUDENDAL/LOCAL ANESTESIA BLOCK TRAY receive FDA 510(k) clearance?

PUDENDAL/LOCAL ANESTESIA BLOCK TRAY received FDA 510(k) clearance on 1988-06-01, under 510(k) number K880988.

Who is the listed applicant for PUDENDAL/LOCAL ANESTESIA BLOCK TRAY?

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 PUDENDAL/LOCAL ANESTESIA BLOCK TRAY?

The FDA product code for PUDENDAL/LOCAL ANESTESIA BLOCK TRAY is KNE.

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Related Devices (Code: KNE)

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

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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