510(k) K223072
K223072 is an FDA 510(k) premarket notification submitted by Pentax of America, Inc. for the device "PENTAX Medical Video Esophagoscope EE17-J10". The FDA issued a decision of Substantially Equivalent on December 2, 2022. The device falls under product code EOX (Esophagoscope (Flexible Or Rigid)), a Class II device regulated under 21 CFR 874.4710. Pentax of America, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 2, 2022
- Date Received
- September 30, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Esophagoscope (Flexible Or Rigid)
- Device Class
- Class II
- Regulation Number
- 874.4710
- Review Panel
- EN
- Submission Type
If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).