Plenity— 510(k) DEN180060

Unknown

Gelesis, Inc.

FDA 510(k) clearance DEN180060 for Plenity, Unknown on 2019-04-12. Applicant: Gelesis, Inc..

Clearance details

Applicant: Gelesis, Inc.
Product code: Code QFQ
Advisory panel: Gastroenterology, Urology
Date received: 2018-11-15
Decision date: 2019-04-12
Decision: Unknown
Clearance type: Direct
Location: Boston, MA, US

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