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FDA 510(k)

PIDURAL STEROID SYSTEM

K-Number: K945484 · 1995-06-02

ApplicantProfessional Medical Device Consultants
Decision Date1995-06-02
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

PIDURAL STEROID SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Professional Medical Device Consultants. It received FDA 510(k) clearance on 1995-06-02 under 510(k) number K945484. 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 PIDURAL STEROID SYSTEM?

PIDURAL STEROID SYSTEM is a medical device that received FDA 510(k) clearance on 1995-06-02. The listed applicant is Professional Medical Device Consultants. The 510(k) number is K945484.

When did PIDURAL STEROID SYSTEM receive FDA 510(k) clearance?

PIDURAL STEROID SYSTEM received FDA 510(k) clearance on 1995-06-02, under 510(k) number K945484.

Who is the listed applicant for PIDURAL STEROID SYSTEM?

The FDA 510(k) record lists Professional Medical Device Consultants as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PIDURAL STEROID SYSTEM?

The FDA product code for PIDURAL STEROID SYSTEM is CAZ.

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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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