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FDA 510(k)

PERIFIX SAFETY EPIDURAL NEEDLES

K-Number: K013610 · 2002-01-25

ApplicantB.Braun Medical, Inc.
Decision Date2002-01-25
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PERIFIX SAFETY EPIDURAL NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2002-01-25 under 510(k) number K013610. 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 PERIFIX SAFETY EPIDURAL NEEDLES?

PERIFIX SAFETY EPIDURAL NEEDLES is a medical device that received FDA 510(k) clearance on 2002-01-25. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K013610.

When did PERIFIX SAFETY EPIDURAL NEEDLES receive FDA 510(k) clearance?

PERIFIX SAFETY EPIDURAL NEEDLES received FDA 510(k) clearance on 2002-01-25, under 510(k) number K013610.

Who is the listed applicant for PERIFIX SAFETY EPIDURAL NEEDLES?

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

What is the FDA product code for PERIFIX SAFETY EPIDURAL NEEDLES?

The FDA product code for PERIFIX SAFETY EPIDURAL NEEDLES is BSP.

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Related Devices (Code: BSP)

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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