Anesthesiology
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- MiscellaneousMiscellaneous
- Subpart B—Diagnostic DevicesCFR Sub-Part
- 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
- FPXStrip, Adhesive, Closure, Skin1Product Code
- FPYSheet, Burn1Product Code
- KGXTape And Bandage, Adhesive1Product Code
- KMFBandage, Liquid1Product Code
- K241916TearRepair Liquid Skin Protectant1Cleared 510(K)
- K182733Rochal Bioshield Silicone Film1Cleared 510(K)
- K171148Aleo BME Liquid Bandage1Cleared 510(K)
- K153571Cavilon Advanced High Endurance Skin Protectant1Cleared 510(K)
- K160684Atteris No-Sting Skin Protectant1Cleared 510(K)
- K131384KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGE1Cleared 510(K)
- K133443MARATHON NO STING LIQUID SKIN PROTECTANT1Cleared 510(K)
- K120059LIQUID BANDAGE1Cleared 510(K)
- K092712SKIN BARRIER FILM1Cleared 510(K)
- K083087ECOCEL1Cleared 510(K)
Show All 223 Submissions
- LRSI.V. Start Kit2Product Code
- MCYWound Dressing Kit2Product Code
- MHWDressing, Compression1Product Code
- NECBandage, Liquid, Skin Protectant1Product Code
- OXQDressing Change Tray1Product Code
- PYOTape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use1Product Code
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
- ToxicologyReview Panel
- Medical GeneticsReview Panel
- UnknownReview Panel
KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGE
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K131384
- 510(k) Type
- Traditional
- Applicant
- KERICURE INC.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 8/7/2014
- Days to Decision
- 450 days
- Submission Type
- Summary