Anesthesiology
Review Panel
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- MiscellaneousMiscellaneous
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart D—Prosthetic DevicesCFR Sub-Part
- HPZImplant, Eye Sphere2Product Code
- HQHEye, Artificial, Non-Custom1Product Code
- HQJImplant, Absorbable, (Scleral Buckling Methods)2Product Code
- HQLIntraocular Lens3Product Code
- HQMKeratoprosthesis, Permanent Implant2Product Code
- HQNConformer, Ophthalmic2Product Code
- K972034MEDPOR OCULAR CONFORMER2Cleared 510(K)
- K970319OCULAR CONFORMER2Cleared 510(K)
- K970318OCULAR CONFORMER2Cleared 510(K)
- K945110KOLBERG OPHTHALMIC CONFORMER2Cleared 510(K)
- K921221STERILE/SINGLE USE SYMBLEPHARON RING2Cleared 510(K)
- K921229STERILE/SINGLE USE OPHTHALMIC CONFORMERS2Cleared 510(K)
- K772168MOLDEYE2Cleared 510(K)
- HQTShell, Scleral2Product Code
- HQWClip, Tantalum, Ophthalmic2Product Code
- HQXImplant, Orbital, Extra-Ocular2Product Code
- KYFImplant, Eye Valve2Product Code
- MFKLens, Multifocal Intraocular3Product Code
- MJPLens, Intraocular, Toric Optics3Product Code
- MLPKeratoprosthesis, Temporary Implant, Surgical Use2Product Code
- MQUOcular Peg2Product Code
- MTZWrap, Implant, Orbital2Product Code
- NAALens, Intraocular, Accommodative3Product Code
- NCKButton, Iris, Eye, Artificial1Product Code
- NFMExpander, Tissue, Orbital2Product Code
- NIZLens, Iris Reconstruction3Product Code
- NQBConformer, Ophthalmic, Biological Tissue2Product Code
- NXMProsthesis, Eyelid Spacer/Graft, Biologic2Product Code
- POEExtended Depth Of Focus Intraocular Lens3Product Code
- PUFOcular Peg, Exempt2Product Code
- PZKLight Adjustable Lens (Lal) And Light Delivery Device (Ldd)3Product Code
- QCBPhakic Toric Intraocular Lens3Product Code
- QWUProsthesis, Eyelid Spacer/Graft, Polymer2Product Code
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—General Hospital and Personal Use Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
- OrthopedicReview Panel
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- General and Plastic SurgeryReview Panel
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MEDPOR OCULAR CONFORMER
- Page Type
- Cleared 510(K)
- 510(k) Number
- K972034
- 510(k) Type
- Traditional
- Applicant
- Porex Surgical, Inc.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 1/20/1998
- Days to Decision
- 232 days
- Submission Type
- Summary