Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate
FDA 510(k) clearance K192017 · decided 2020-04-24
Clearance details
- K-number
- K192017
- Device name
- Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate
- Applicant
- Fresenius Medical Care Renal Therapies Group, LLC
- Decision
- Substantially Equivalent
- Date received
- 2019-07-29
- Decision date
- 2020-04-24
- Days to decision
- 270 days
- Clearance type
- Traditional
- Product code
- KPO
- Device class
- 2
- Regulation number
- 876.5820
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Waltham, MA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.