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

OTC12D AUTO RADIOGRAPHIC SYSTEM

K Number: K152767 · Decision Dec 14, 2015
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
4
Review Days
81

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
OTC12D AUTO RADIOGRAPHIC SYSTEM
K Number
K152767
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Del Medical, Inc.
Date Received
September 24, 2015
Decision Date
December 14, 2015
Product Code
KPR
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
KPR System, X-Ray, Stationary

Similar 510(k) Clearances

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

View all

Other Clearances by Del Medical, Inc.

K Number Device Name
K223550 DMX
K173018 MDR17 Mobile Direct Radiographic System
K140825 DELWORKS DR SYSTEM