Atlas FDA

Obalon Touch Dispenser

FDA premarket approval P160001/S036 · decided 2019-04-26

Approval details

PMA number
P160001
Supplement
S036
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
2019-03-29
Decision date
2019-04-26
Days to decision
28 days
Decision code
OK30
Product code
LTI
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Eden Prairie, MN
Statement
to add an inspection step for the Touch DispenserÂ’s manifold

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