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

MYVACET 5-07, 7-00 AND 9-40

K Number: K791178 · Decision Sep 17, 1979
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
50
Applicant Total
8
Review Days
84

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
MYVACET 5-07, 7-00 AND 9-40
K Number
K791178
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Radiation Products Design, Inc.
Date Received
June 25, 1979
Decision Date
September 17, 1979
Product Code
IXI
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
IXI Block, Beam-Shaping, Radiation Therapy

Similar 510(k) Clearances

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

View all

Other Clearances by Radiation Products Design, Inc.

K Number Device Name
K150382 Radio Therapy Treatment Chair
K800760 BITE BLOCK SYSTEM
K800761 POINT TO POINT LEVEL
K800759 ELEV. BACK SUPPORT W/ADJ. ARM POSITIONER
K800792 ADJUSTABLE HEAD & FACE HOLDER
K800791 MYLAR WINDOW-TABLE INSERT PANEL
K800790 TENNIS RACKET-TABLE INSERT PANEL