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

PLANMED NUANCE EXCEL

K Number: K111361 · Decision Sep 23, 2011
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
54
Applicant Total
13
Review Days
130

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
PLANMED NUANCE EXCEL
K Number
K111361
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1715
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Planmeca USA, Inc.
Date Received
May 16, 2011
Decision Date
September 23, 2011
Product Code
MUE
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
MUE Full Field Digital, System, X-Ray, Mammographic

Similar 510(k) Clearances

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

View all

Other Clearances by Planmeca USA, Inc.

K Number Device Name
K081699 PLANMECA SOVEREIGN
K923534 PM2002 PROLINE
K923533 ADMARK
K923462 DELIGHT
K923461 PM2002 PROLINE, PM2002 PROLINE EC
K904953 PLANMED SOPHIE
K904947 PM2002 CC, ARISTOCRAT AND ARISTOCRAT DELUXE
K904948 PM2002 CC AND PM2002 EC
K864474 DENTAL RADIOGRAPHIC 90, MODEL PM 2002 CC PANORAMIC
K842359 AUTOMATIC PATIENT CHAIR PM2000 & A
Search all 13 clearances from Planmeca USA, Inc. →