Anesthesiology
Review Panel
- CardiovascularReview Panel
- ChemistryReview Panel
- DentalReview Panel
- MiscellaneousMiscellaneous
- LTGPaste, Injectable For Vocal Cord Augmentation3Product Code
- LWMDevice, Electrical Dental AnesthesiaUProduct Code
- MCLKit, Test, In Vitro Periodontal3Product Code
- MQCMouthguard, PrescriptionUProduct Code
- MVLCord, RetractionUProduct Code
- K211420Stasis GelUCleared 510(K)
- K211419Gingi-Aid GelUCleared 510(K)
- K213149VOCO Retraction PasteUCleared 510(K)
- K200764STATSTIXUCleared 510(K)
- K193389Vista ClearUCleared 510(K)
- K190220Vista FS, Vista FS LiquidUCleared 510(K)
- K171577Smartcord, Smartcord XUCleared 510(K)
- K162662GingiDent Gingival Retraction PasteUCleared 510(K)
- K162948Styptin, Hemogin-L, Hemodettes, and GingiGEL Aluminum Chloride Impregnated Retraction Cord/MaterialsUCleared 510(K)
- K162536GingiKnit+, GingiBraid+, GingiBraid+ Shortcut, and UniBraid+ impregnated Aluminum Potassium Sulfate Retraction CordUCleared 510(K)
- K162164GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction CordUCleared 510(K)
- K152064Astringedent ClearUCleared 510(K)
- K150423EXPAZENUCleared 510(K)
- K130580RETRACTION PASTEUCleared 510(K)
- K131799QUICKNITUCleared 510(K)
- K132526KNIT-PAK+UCleared 510(K)
- K123215VISCOSTAT CLEARUCleared 510(K)
- K113839RETRACT GINGIVAL RETRACTION/HEMOSTATIC PASTEUCleared 510(K)
- K111978SULCUS BLUEUCleared 510(K)
- K111348RE / STASIS (TM) GINGIVAL RETRACTION PASTEUCleared 510(K)
- K101756TSCUCleared 510(K)
- K102133GIRAFFE2UCleared 510(K)
- K093721COSP2UCleared 510(K)
- K093711RACEGELUCleared 510(K)
- K092384LIQUICORDUCleared 510(K)
- K091380CORDCAPUCleared 510(K)
- K083695TRAXODENTUCleared 510(K)
- K082116HEMOSTASYL PASTEUCleared 510(K)
- K053329KORLEX-GR GINGIVAL RETRACTION PASTEUCleared 510(K)
- K050180EXPA-SYLUCleared 510(K)
- K041023STAY-PUT IMPREGNATEDUCleared 510(K)
- K010070ULTRAPAK NEHAUCleared 510(K)
- K981596ULTRAPAK EUCleared 510(K)
- QMJPowered Radiofrequency Toothbrush2Product Code
- QNONeuromuscular Tongue Muscle Stimulator For The Reduction Of Snoring And Obstructive Sleep Apnea2Product Code
- KJJCleanser, Root CanalUProduct Code
- LFDSaliva, ArtificialUProduct Code
- LMWSolution, Removal, Carries3Product Code
- LPGMaterial, Dressing, Surgical, Polylactic Acid3Product Code
- LQYLocator, Root ApexUProduct Code
- NSJRestoration, Noble MetalNProduct Code
- NSKDentures, PartialNProduct Code
- NSLDentures, FullNProduct Code
- NSMRestoration, ResinNProduct Code
- NSNRestoration, Resin, Crown And BridgeNProduct Code
- NSORestoration, Porcelain-Fused-To-MetalNProduct Code
- NSPRestoration, PorcelainNProduct Code
- NSQRestoration, Base MetalNProduct Code
- NSRProsthesis, OrthodonticNProduct Code
- NXJDenture, Cosmetic OnlyNProduct Code
- OBRMouthguard, Over-The-CounterUProduct Code
- OCOMouthguard, Migraine/Tension HeadacheUProduct Code
- OLROral Wound DressingUProduct Code
- OLSOral Wound Dressing W/Drug And/Or BiologicUProduct Code
- PKJCrown And Bridge Material, Resin BasedNProduct Code
- QUAIntraoral Cooling Device2Product Code
- Submissions with No Product CodeMiscellaneous
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart B—Physical Medicine Diagnostic DevicesCFR Sub-Part
- Subpart D—Physical Medicine Prosthetic DevicesCFR Sub-Part
- Subpart D—Prosthetic DevicesCFR Sub-Part
- Subpart E—Surgical 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
- Subpart G—Miscellaneous DevicesCFR Sub-Part
- Ear, Nose, ThroatReview Panel
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- NeurologyReview Panel
- Obstetrical and GynecologicalReview Panel
- OphthalmicReview Panel
- OrthopedicReview Panel
- PathologyReview Panel
- Physical MedicineReview Panel
- RadiologyReview Panel
- General and Plastic SurgeryReview Panel
- ToxicologyReview Panel
- Medical GeneticsReview Panel
- UnknownReview Panel
LIQUICORD
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K092384
- 510(k) Type
- Traditional
- Applicant
- CENTRIX, INC.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 11/4/2009
- Days to Decision
- 91 days
- Submission Type
- Statement