Obalon Touch Dispenser
FDA premarket approval P160001/S039 · decided 2019-08-20
Approval details
- PMA number
- P160001
- Supplement
- S039
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- Obalon Touch Dispenser
- Generic name
- IMPLANT, INTRAGASTRIC FOR MORBID OBESITY
- Applicant
- Medtimo, Inc.
- Date received
- 2019-05-24
- Decision date
- 2019-08-20
- Days to decision
- 88 days
- Decision code
- APPR
- Product code
- LTI
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Eden Prairie, MN
- Statement
- Approval for updating the Touch Dispenser software to disable the touchscreen recalibration functionality.
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