2akhi107

FCC ID

Equipment:

Pentax Medical 107

303 Convention Way STE 1, REDWOOD CITY, CA 94063 United States

Application
Frequency Range
Final Action Date
Granted
xYtCKAuqo3NYmaKjrm6TJA==
13.56-13.56
2021-12-15
APPROVED
File NameDocument TypeDateDirect
Extracted Label GraphicID Label/Location Info 2021-12-15 00:00:00 pdf
Manual Rev 2Users Manual 2022-06-07 00:00:00 pdf
SetupTest Setup Photos 2021-12-15 00:00:00 pdf
Test ReportTest Report 2021-12-15 00:00:00 pdf
RFxRF Exposure Info 2021-12-15 00:00:00 pdf
IntInternal Photos 2022-06-07 00:00:00 pdf
ExtExternal Photos 2021-12-15 00:00:00 pdf
AuthorizationCover Letter(s) 2021-12-15 00:00:00 pdf
LocationID Label/Location Info 2021-12-15 00:00:00 pdf
Confid RequestCover Letter(s) 2021-12-15 00:00:00 pdf
BlockBlock Diagram N/A
OpsOperational Description N/A
DatasheetOperational Description N/A
MainSchematics N/A
SensorSchematics N/A

Application Details:

EquipmentC2 CryoBallon Ablation System
FRN0026046078
Grantee Code2AKHI
Product Code-107
Applicant BusinessPentax Medical
Business Address303 Convention Way STE 1, REDWOOD CITY,California United States 94063
TCB ScopeA1: Low Power Transmitters below 1 GHz (except Spread Spectrum), Unintentional Radiators, EAS (Part 11) & Consumer ISM devices
TCB Email[email protected]
ApplicantGurvinder Singh Nanda – Sr. Director Regulatory and Quality
Applicant Phone
Applicant Fax6503168601
Applicant Email[email protected]
Applicant MailStop
Test FirmTUV Rheinland of North America Inc.
Test Firm ContactDavid Spencer
Test Firm Phone
Test Firm Fax925 249 9124
Test Firm Email[email protected]
Certified ByGurvinder Singh Nanda – Sr Director of Regulatory Affairs

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