Anesthesiology
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- MiscellaneousMiscellaneous
- Subpart B—Diagnostic DevicesCFR Sub-Part
- GCILaryngoscope, Endoscope2Product Code
- GCJLaparoscope, General & Plastic Surgery2Product Code
- MFJDevice, Endoscopic Suturing2Product Code
- EPYSpeculum, Ent1Product Code
- NAYSystem, Surgical, Computer Controlled Instrument2Product Code
- NEQDevice, Telemedicine, Robotic2Product Code
- PDTBurn Resuscitation Decision Support Software2Product Code
- FDPApparatus, Pneumoperitoneum, Automatic2Product Code
- GCGPeritoneoscope2Product Code
- GCHMediastinoscope, Diagnostic2Product Code
- OTJLaparoscopic Single Port Access Device2Product Code
- K232062Uni-port2Cleared 510(K)
- K220081CORE-SPORT2Cleared 510(K)
- K202688AFS Medical Sterile Single-Use Access Port System2Cleared 510(K)
- K160797FMX314 Surgical Platform2Cleared 510(K)
- K152598Endo Keeper2Cleared 510(K)
- K121309ASC QUADPORT + LAPAROSCOPIC ACCESS DEVICE2Cleared 510(K)
- K120898KEYPORT SYSTEM, INCLUDES: KEYPORT SILICONE SEALING INSERT 8850XXX KEYPORT TRUCAR 8850XX KEYPORT TROCAR 8850XX SEALING CA2Cleared 510(K)
- K111407TRIPORT, TRIPORT+, TRIPORT15, QUADPORT2Cleared 510(K)
- K112196OCTOTMPORT2Cleared 510(K)
- K110004ASC TRIPORT+ LAPAROSCOPIC ACCESS DEVICE2Cleared 510(K)
Show All 11 Submissions
- OWNConfocal Optical Imaging2Product Code
- QGYMobile / Tablet Software Application To Control Settings Of Surgical And Endoscopic Camera2Product Code
- NQQSystem, Imaging, Optical Coherence Tomography (Oct)2Product Code
- POYPost Breast Biopsy Hemostatic Breast Compression Device2Product Code
- FXESpeculum, Non-Illuminated1Product Code
- FXFSpeculum, Illuminated1Product Code
- FXGSpecula Accessories1Product Code
- JYKHolder, Ear Speculum1Product Code
- KAGHolder, Speculum, Ent1Product Code
- QSMSystem, Surgical, Computer Controlled Instrument, Remanufactured2Product Code
- QZBSoftware Controlled Endoscope And Instrument Holder2Product Code
- Subpart C—General Hospital and Personal Use Monitoring DevicesCFR Sub-Part
- Subpart D—Prosthetic DevicesCFR Sub-Part
- Subpart E—Neurological Surgical DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—General Hospital and Personal Use Therapeutic DevicesCFR Sub-Part
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
- ToxicologyReview Panel
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- UnknownReview Panel
AFS Medical Sterile Single-Use Access Port System
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K202688
- 510(k) Type
- Traditional
- Applicant
- AFS Medical Co. Ltd.
- Country
- South Korea
- FDA Decision
- Substantially Equivalent
- Decision Date
- 10/14/2021
- Days to Decision
- 394 days
- Submission Type
- Summary