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FDA 510(k)

PENCIL POINT SPINAL NEEDLE AND TRAY

K-Number: K932569 · 1994-01-26

ApplicantB. Braun of America, Inc.
Decision Date1994-01-26
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PENCIL POINT SPINAL NEEDLE AND TRAY is the device name listed in this FDA 510(k) record. The listed applicant is B. Braun of America, Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K932569. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENCIL POINT SPINAL NEEDLE AND TRAY?

PENCIL POINT SPINAL NEEDLE AND TRAY is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is B. Braun of America, Inc.. The 510(k) number is K932569.

When did PENCIL POINT SPINAL NEEDLE AND TRAY receive FDA 510(k) clearance?

PENCIL POINT SPINAL NEEDLE AND TRAY received FDA 510(k) clearance on 1994-01-26, under 510(k) number K932569.

Who is the listed applicant for PENCIL POINT SPINAL NEEDLE AND TRAY?

The FDA 510(k) record lists B. Braun of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PENCIL POINT SPINAL NEEDLE AND TRAY?

The FDA product code for PENCIL POINT SPINAL NEEDLE AND TRAY is BSP.

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Other records listing B. Braun of America, Inc. as applicant

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Related Devices (Code: BSP)

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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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