FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MVP (MULTI-VENDOR PROTOCOL CONVERTOR)
K Number: K900227
·
Decision Feb 12, 1990
Classifications
1
FEI Numbers
148
Registration Numbers
148
Same Product Code
141
Applicant Total
1
Review Days
26
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- MVP (MULTI-VENDOR PROTOCOL CONVERTOR)
- K Number
- K900227
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 892.2020
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Merge Technologies, Inc.
- Date Received
- January 17, 1990
- Decision Date
- February 12, 1990
- Product Code
- LMD
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LMD | System, Digital Image Communications, Radiological | FDA class 1 | Radiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (LMD), ordered by most recent decision date.
IIVS INTEGRATED IMAGE VIEWING STATION
FDA 510(k)
FDA Class 1
·Radiology
STENTOR, PAGEVIEW
FDA 510(k)
FDA Class 1
·Radiology
RAYPAX WEB CLINICAL SYSTEM
FDA 510(k)
FDA Class 1
·Radiology
ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0
FDA 510(k)
FDA Class 1
·Radiology
SAMSUNG RAYPAX SYSTEM
FDA 510(k)
FDA Class 1
·Radiology
STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEM
FDA 510(k)
FDA Class 1
·Radiology