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FDA 510(k)

MICROVISION SCLERAL BUCKLING COMPONENTS

K-Number: K023481 · 2003-01-08

ApplicantMicrovision, Inc.
Decision Date2003-01-08
Product CodeHQX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MICROVISION SCLERAL BUCKLING COMPONENTS is the device name listed in this FDA 510(k) record. The listed applicant is Microvision, Inc.. It received FDA 510(k) clearance on 2003-01-08 under 510(k) number K023481. The device is classified under product code HQX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROVISION SCLERAL BUCKLING COMPONENTS?

MICROVISION SCLERAL BUCKLING COMPONENTS is a medical device that received FDA 510(k) clearance on 2003-01-08. The listed applicant is Microvision, Inc.. The 510(k) number is K023481.

When did MICROVISION SCLERAL BUCKLING COMPONENTS receive FDA 510(k) clearance?

MICROVISION SCLERAL BUCKLING COMPONENTS received FDA 510(k) clearance on 2003-01-08, under 510(k) number K023481.

Who is the listed applicant for MICROVISION SCLERAL BUCKLING COMPONENTS?

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

What is the FDA product code for MICROVISION SCLERAL BUCKLING COMPONENTS?

The FDA product code for MICROVISION SCLERAL BUCKLING COMPONENTS is HQX.

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.

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Other records listing Microvision, 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.

K022186SCLERAL PLUGS, 19 AND 20 GAUGEK982462FIBER OPTIC ENDOILLUMINATION PROBE

Related Devices (Code: HQX)

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.

K983581OCU-GUARD AND OCU-GUARD SUPPLEBio-Vascular, Inc.K980816RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGESFci Ophthalmics, Inc.K963219RETINAL DETACHMENT IMPLANTS; INCLUDING BANS, STRIPS, TIRES, SLEEVES, CORDS AND SPONGESFci Ophthalmics, Inc.K950806SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTSMira, Inc.K950599STORS SCLERAL SPONGE II (LINCOFF DESIGN)Storz Ophthalmics, Inc.K945172VISITEC SILICONE RETINAL IMPLANTS/EXPLANTSVisitec Co.

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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