FDA 510(k) Substantially Equivalent 🇺🇸 United States

VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER

K Number: K827577 · Decision Jan 24, 1983
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
6
Review Days
35

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
VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER
K Number
K827577
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Randwal Instrument Co., Inc.
Date Received
December 20, 1982
Decision Date
January 24, 1983
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

Other Clearances by Randwal Instrument Co., Inc.

K Number Device Name
K873990 IRAS EDS INTERFEROMETRIC STIMULATOR
K873987 IRAS GLARE TESTER
K864012 IRAS PERIMETER
K853556 LASER IRAS
K842567 PORTABLE ACUIOMETER