Atlas FDA

RECTILINEAR SCANNER MODEL #187-270

FDA 510(k) clearance K895799 · decided 1990-02-01

Clearance details

K-number
K895799
Device name
RECTILINEAR SCANNER MODEL #187-270
Applicant
Atomic Products Corp.
Decision
Substantially Equivalent
Date received
1989-09-28
Decision date
1990-02-01
Days to decision
126 days
Clearance type
Traditional
Product code
IYW
Device class
1
Regulation number
892.1300
Medical specialty
Radiology
Advisory committee
Radiology
Location
Shirley, NY, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
POLYSCAN DIGITAL SCANNER (K944684)Mse Medizintechnik GmbH & Co. KG1995-05-15
POLYSCAN DIGITAL SCANNER (K882453)Medical and Scientific Enterprises, Inc.1988-11-23
IMAGER, BODY SECTION, RADIONUCLIDE (K780395)Union Carbide Corp.1978-03-31

Recalls involving this device

No recalls on record reference this clearance.