Atlas FDA

Mahana Parallel Digital Cognitive Behavioral Therapy (CBT) Mobile Application for Irritable Bowel Syndrome (IBS)

FDA 510(k) clearance K211372 · decided 2021-06-02

Clearance details

K-number
K211372
Device name
Mahana Parallel Digital Cognitive Behavioral Therapy (CBT) Mobile Application for Irritable Bowel Syndrome (IBS)
Applicant
Mahana Therapeutics, Inc.
Decision
Substantially Equivalent
Date received
2021-05-04
Decision date
2021-06-02
Days to decision
29 days
Clearance type
Special
Product code
QMY
Device class
2
Regulation number
876.5960
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
San Francisco, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Regulora (K211463)Metame Health, Inc.2021-11-24
Parallel (DEN200029)Mahana Therapeutics, Inc.2020-11-25

Recalls involving this device

No recalls on record reference this clearance.