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FDA 510(k)

WEISS RETINAL CANNULA

K-Number: K010305 · 2001-05-02

Decision Date2001-05-02
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WEISS RETINAL CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Micron Surgical, Inc.. It received FDA 510(k) clearance on 2001-05-02 under 510(k) number K010305. The device is classified under product code HMX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WEISS RETINAL CANNULA?

WEISS RETINAL CANNULA is a medical device that received FDA 510(k) clearance on 2001-05-02. The listed applicant is Micron Surgical, Inc.. The 510(k) number is K010305.

When did WEISS RETINAL CANNULA receive FDA 510(k) clearance?

WEISS RETINAL CANNULA received FDA 510(k) clearance on 2001-05-02, under 510(k) number K010305.

Who is the listed applicant for WEISS RETINAL CANNULA?

The FDA 510(k) record lists Micron Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WEISS RETINAL CANNULA?

The FDA product code for WEISS RETINAL CANNULA is HMX.

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.

Related Devices (Code: HMX)

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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