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

Ion Endoluminal System (IF1000)

K Number: K252528 · Decision Sep 5, 2025
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
238
Applicant Total
176
Review Days
25

Basic Information

Device Name
Ion Endoluminal System (IF1000)
K Number
K252528
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intuitive Surgical, Inc.
Date Received
August 11, 2025
Decision Date
September 5, 2025
Product Code
EOQ
Advisory Committee
Ear, Nose, Throat
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
EOQ Bronchoscope (Flexible Or Rigid)

Similar 510(k) Clearances

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

View all

Other Clearances by Intuitive Surgical, Inc.

K Number Device Name
K253986 da Vinci Force Feedback Instruments
K253978 Universal Seal (5-12 mm)
K251739 da Vinci Surgical System (IS5000)
K253556 da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator
K251763 IRISeg
K252675 da Vinci SP Surgical System (SP1098)
K252069 da Vinci SP Surgical System (SP1098)
K251426 da Vinci SP Surgical System (SP1098)
K252045 Ion Endoluminal System (IF1000)
K251817 da Vinci SP Surgical System (SP1098)
Search all 176 clearances from Intuitive Surgical, Inc. →