Anesthesiology
Review Panel
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- ChemistryReview Panel
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- Gastroenterology and UrologyReview Panel
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- HematologyReview Panel
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- MiscellaneousMiscellaneous
- Subpart B—Cardiovascular Diagnostic DevicesCFR Sub-Part
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart B—Neurological Diagnostic DevicesCFR Sub-Part
- Subpart B—Physical Medicine Diagnostic DevicesCFR Sub-Part
- Subpart C—Cardiovascular Monitoring DevicesCFR Sub-Part
- Subpart D—Physical Medicine Prosthetic DevicesCFR Sub-Part
- Subpart E—Neurological Surgical DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—Cardiovascular Therapeutic DevicesCFR Sub-Part
- NCXSystem, Hypothermia, Intravenous, Cooling2Product Code
- K223746Solex 7 Intravascular Heat Exchange Catheter, Cool Line Intravascular Heat Exchange Catheter, ICY Intravascular Heat Exchange Catheter, Quattro Intravascular Heat Exchange Catheter, Thermogard XP Console, Thermogard HQ Console2Cleared 510(K)
- K220008Solex 7 Intravascular Heat Exchange Catheter, Cool Line Intravascular Heat Exchange Catheter, ICY Intravascular Heat Exchange Catheter, Quattro Intravascular Heat Exchange Catheter, Thermogard HQ Start-Up Kit, Thermogard HQ Start-Up Kit EX, Thermogard HQ Console2Cleared 510(K)
- K213031Solex 7 Intravascular Heat Exchange Catheter, Cool Line Intravascular Heat Exchange Catheter, ICY Intravascular Heat Exchange Catheter, Quattro Intravascular Heat Exchange Catheter, Start-Up Kit, Coolgard 3000 Console, Thermogard XP Console2Cleared 510(K)
- K152946TEMPEDY2Cleared 510(K)
- K153162Hypocore2Cleared 510(K)
- K153226Solex 7 Intravascular Heat Exchange Catheter, ZOLL Start-Up Kit2Cleared 510(K)
- K150046Start-Up Kit (SUK), Cool Line Intravascular Heat Exchange Catheter, ICY Intravascular Heat Exchange Catheter, Quattro Intravascular Heat Exchange Catheter2Cleared 510(K)
- K141139SOLEX INTRAVASCULAR HEAT EXCHANGE CATHETER2Cleared 510(K)
- K101987COOL LINE CATHETER, MODEL CL-2295A, ICY CATHETER, MODEL IC-3893A AND QUATTRO CATHETER, MODEL IC-45932Cleared 510(K)
- K080908INNERCOOL THERAPIES, INC., RAPIDBLUE SYSTEM2Cleared 510(K)
Show All 26 Submissions
- Subpart F—Neurological Therapeutic DevicesCFR Sub-Part
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
- Obstetrical and GynecologicalReview Panel
- OphthalmicReview Panel
- OrthopedicReview Panel
- PathologyReview Panel
- Physical MedicineReview Panel
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- General and Plastic SurgeryReview Panel
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- UnknownReview Panel
TEMPEDY
- Page Type
- Cleared 510(K)
- 510(k) Number
- K152946
- 510(k) Type
- Traditional
- Applicant
- Seiratherm GmbH
- Country
- Germany
- FDA Decision
- Substantially Equivalent
- Decision Date
- 9/15/2016
- Days to Decision
- 345 days
- Submission Type
- Summary