PROTEUS INGESTION CONFINMATION SYSTEMS— 510(k) DEN120011

Name: FDA 510(k) clearance DEN120011
Creator: U.S. Food and Drug Administration
Published: 2012-07-10

Unknown

Proteus Biomedical, Inc.

FDA 510(k) clearance DEN120011 for PROTEUS INGESTION CONFINMATION SYSTEMS, Unknown on 2012-07-10. Applicant: Proteus Biomedical, Inc.. Device class: 2.

Clearance details

Applicant: Proteus Biomedical, Inc.
Product code: Code OZW
Device class: Class 2
Regulation: 21 CFR 880.6305
Advisory panel: General Hospital
Date received: 2012-05-11
Decision date: 2012-07-10
Decision: Unknown
Clearance type: Post-NSE
Location: Redwood City, CA, US

View on FDA.gov ↗

Recent devices under product code OZW

view all

K251088 — Otsuka Digital Feedback Device2025-06-30
K223463 — Otsuka Digital Feedback Device-RW2023-08-11
K183052 — ID-Cap System2019-12-06
K150494 — Proteus Digital Health Feedback Device2015-06-27
K133263 — PROTEUS PATCH, PROTEUS INGESTIBLE SENSOR (ACCESSORY)2014-02-07

More clearances from Proteus Biomedical, Inc.

view all

K093976 — RAISIN PERSONAL MONITOR2010-03-25

Data sourced from openFDA. This site is unofficial and independent of the FDA.