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FDA 510(k)

EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS

K-Number: K991719 · 1999-08-18

ApplicantMedimex Holfeld GmbH & Co.
Decision Date1999-08-18
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Medimex Holfeld GmbH & Co.. It received FDA 510(k) clearance on 1999-08-18 under 510(k) number K991719. 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 EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS?

EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS is a medical device that received FDA 510(k) clearance on 1999-08-18. The listed applicant is Medimex Holfeld GmbH & Co.. The 510(k) number is K991719.

When did EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS receive FDA 510(k) clearance?

EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS received FDA 510(k) clearance on 1999-08-18, under 510(k) number K991719.

Who is the listed applicant for EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS?

The FDA 510(k) record lists Medimex Holfeld GmbH & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS?

The FDA product code for EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS 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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