Midmark Extraoral Imaging System (EOIS)— 510(k) K201667
Substantially EquivalentMidmark Corporation
FDA 510(k) clearance K201667 for Midmark Extraoral Imaging System (EOIS), Substantially Equivalent on 2020-08-06. Applicant: Midmark Corporation. Device class: 2.
Clearance details
- Applicant
- Midmark Corporation
- Product code
- Code OAS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1750
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Buffalo Grove, IL, US
Recent devices under product code OAS
view allMore clearances from Midmark Corporation
view all- K253196 — Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)
- K251626 — Midmark Dental Delivery System
- K233026 — Midmark Smart M9® Sterilizer, Midmark Smart M11® Sterilizer
- K163337 — Midmark and Ritter M9 and M11 UltraClave® Automatic Sterilizers and Ritter M9D AutoClave® Automatic Sterilizer
- K161909 — IQvitals Zone
Data sourced from openFDA. This site is unofficial and independent of the FDA.