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FDA 510(k)

MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE

K-Number: K962736 · 1996-07-29

Decision Date1996-07-29
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Mill-Rose Laboratory. It received FDA 510(k) clearance on 1996-07-29 under 510(k) number K962736. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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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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