Atlas FDA

POLYSCAN DIGITAL SCANNER

FDA 510(k) clearance K882453 · decided 1988-11-23

Clearance details

K-number
K882453
Device name
POLYSCAN DIGITAL SCANNER
Applicant
Medical and Scientific Enterprises, Inc.
Decision
Substantially Equivalent
Date received
1988-06-14
Decision date
1988-11-23
Days to decision
162 days
Clearance type
Traditional
Product code
IYW
Device class
1
Regulation number
892.1300
Medical specialty
Radiology
Advisory committee
Radiology
Location
Sudbury, MA, 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
RECTILINEAR SCANNER MODEL #187-270 (K895799)Atomic Products Corp.1990-02-01
IMAGER, BODY SECTION, RADIONUCLIDE (K780395)Union Carbide Corp.1978-03-31

Recalls involving this device

No recalls on record reference this clearance.