FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

EXCELVIEW ILLUMINATOR

K Number: K883702 · Decision Sep 19, 1988
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
17
Applicant Total
2
Review Days
20

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
EXCELVIEW ILLUMINATOR
K Number
K883702
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1890
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Excel Medical Products, Inc.
Date Received
August 30, 1988
Decision Date
September 19, 1988
Product Code
IXC
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
IXC Illuminator, Radiographic-Film

Similar 510(k) Clearances

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

View all

Other Clearances by Excel Medical Products, Inc.

K Number Device Name
K883357 MODEL 1080 ROLLER MASSAGE TABLE