EPIDURAL ANESTHESIA PROCEDURE TRAY, CUSTOM
K-Number: K933721 · 1994-01-31
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Device Summary
Frequently Asked Questions
What is the EPIDURAL ANESTHESIA PROCEDURE TRAY, CUSTOM?
EPIDURAL ANESTHESIA PROCEDURE TRAY, CUSTOM is a medical device that received FDA 510(k) clearance on 1994-01-31. The listed applicant is Neurodelivery Technology, Inc.. The 510(k) number is K933721.
When did EPIDURAL ANESTHESIA PROCEDURE TRAY, CUSTOM receive FDA 510(k) clearance?
EPIDURAL ANESTHESIA PROCEDURE TRAY, CUSTOM received FDA 510(k) clearance on 1994-01-31, under 510(k) number K933721.
Who is the listed applicant for EPIDURAL ANESTHESIA PROCEDURE TRAY, CUSTOM?
The FDA 510(k) record lists Neurodelivery Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EPIDURAL ANESTHESIA PROCEDURE TRAY, CUSTOM?
The FDA product code for EPIDURAL ANESTHESIA PROCEDURE TRAY, CUSTOM is CAZ.
Related Clinical Trials
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.
Other records listing Neurodelivery Technology, Inc. as applicant
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.
Related Devices (Code: CAZ)
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.
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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