MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE
K-Number: K962736 · 1996-07-29
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Device Summary
Frequently Asked Questions
What is the MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE?
MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE is a medical device that received FDA 510(k) clearance on 1996-07-29. The listed applicant is Mill-Rose Laboratory. The 510(k) number is K962736.
When did MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE receive FDA 510(k) clearance?
MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE received FDA 510(k) clearance on 1996-07-29, under 510(k) number K962736.
Who is the listed applicant for MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE?
The FDA 510(k) record lists Mill-Rose Laboratory as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE?
The FDA product code for MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE is EOQ.
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 Mill-Rose Laboratory 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: EOQ)
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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