CRYSTALVIEW R200— 510(k) K062390
Substantially EquivalentAlara, Inc.
FDA 510(k) clearance K062390 for CRYSTALVIEW R200, Substantially Equivalent on 2006-09-18. Applicant: Alara, Inc.. Device class: 2.
Clearance details
- Applicant
- Alara, Inc.
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Fremont, CA, US
Recent devices under product code MQB
view allMore clearances from Alara, Inc.
view all- K102479 — ALARA T210 COMPUTED RADIOGRAPHY SYSTEM
- K071682 — CRYSTALVIEW T-SERIES COMPUTED RADIOGRAPHY SYSTEM, MODELS T110 (WITH ERASER) AND T100 (WITHOUT ERASER)
- K061538 — ALARA CRYSTALVIEW COMPUTED RADIOGRAPHY SYSTEM, MODEL R200
- K032210 — ALARA CRYSTALVIEW COMPUTED RADIOGRAPHY SYSTEM
- K000162 — METRISCAN BONE DENSITY SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.