Anesthesiology
Review Panel
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- ChemistryReview Panel
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- MiscellaneousMiscellaneous
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart B—Obstetrical and Gynecological Diagnostic DevicesCFR Sub-Part
- Subpart C—Cardiovascular Monitoring DevicesCFR Sub-Part
- Subpart C—Monitoring DevicesCFR Sub-Part
- Subpart D—Prosthetic DevicesCFR Sub-Part
- FAEProsthesis, Penile2Product Code
- FAFProsthesis, Testicular3Product Code
- FHWDevice, Impotence, Mechanical/Hydraulic3Product Code
- FTOProsthesis, Testicle3Product Code
- FTQProsthesis, Penis, Rigid Rod2Product Code
- JCWProsthesis, Penis, Inflatable3Product Code
- QGAPenile Implant Surgical Accessories1Product Code
- ESWProsthesis, Esophageal2Product Code
- K233939Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent System2Cleared 510(K)
- K233837Agile Esophageal Stent System2Cleared 510(K)
- K240522Esophageal TTS Stent2Cleared 510(K)
- K223266Hilzo Esophageal Stents2Cleared 510(K)
- K221482Esophageal TTS Stent2Cleared 510(K)
- K211960Agile Esophageal OTW Stent System2Cleared 510(K)
- K213251HANAROSTENT Esophagus Asymmetric (CCC)2Cleared 510(K)
- K211706Esophageal TTS Stent2Cleared 510(K)
- K201160HANAROSTENT Esophagus (CCC), HANAROSTENT Esophagus (NCN)2Cleared 510(K)
- K200860HANAROSTENT Esophagus TTS (CCC), HANAROSTENT Esophagus TTS (NCN)2Cleared 510(K)
Show All 56 Submissions
- MQRStent, Colonic, Metallic, Expandable2Product Code
- MUMStent, Metallic, Expandable, Duodenal2Product Code
- OTMMesh, Surgical, For Stress Urinary Incontinence, Male2Product Code
- OTNMesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator2Product Code
- PAGMesh, Surgical, Non-Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator2Product Code
- PAHMesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-Sling2Product Code
- Subpart E—Obstetrical and Gynecological Surgical DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—Neurological Therapeutic DevicesCFR Sub-Part
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
- Subpart G—General Hospital and Personal Use Miscellaneous DevicesCFR Sub-Part
- General HospitalReview Panel
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- Obstetrical and GynecologicalReview Panel
- OphthalmicReview Panel
- OrthopedicReview Panel
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HANAROSTENT Esophagus TTS (CCC), HANAROSTENT Esophagus TTS (NCN)
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K200860
- 510(k) Type
- Traditional
- Applicant
- M.I. Tech Co., Ltd
- Country
- South Korea
- FDA Decision
- Substantially Equivalent
- Decision Date
- 5/20/2020
- Days to Decision
- 49 days
- Submission Type
- Summary