FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Bongo

K Number: K180619 · Decision Aug 16, 2018
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
4
Applicant Total
1
Review Days
160

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Bongo
K Number
K180619
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5570
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innomed Healthscience, Inc.
Date Received
March 9, 2018
Decision Date
August 16, 2018
Product Code
OHP
Advisory Committee
Dental
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OHP Expiratory Resistance Valve, Intranasal, For Obstructive Sleep Apnea

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OHP), ordered by most recent decision date.

View all