Obalon Touch Dispenser
FDA premarket approval P160001/S040 · decided 2019-07-03
Approval details
- PMA number
- P160001
- Supplement
- S040
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Obalon Touch Dispenser
- Generic name
- IMPLANT, INTRAGASTRIC FOR MORBID OBESITY
- Applicant
- Medtimo, Inc.
- Date received
- 2019-06-03
- Decision date
- 2019-07-03
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- LTI
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Eden Prairie, MN
- Statement
- Change high pressure regulator and low pressure regulator target setpoints, the final release testing acceptance criteria for the regulator pressures, and the associated in-process and final acceptance activities.
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