Atlas FDA

DIGITAL RADIOGRAPHY SYSTEM

FDA 510(k) clearance K827289 · decided 1982-04-21

Clearance details

K-number
K827289
Device name
DIGITAL RADIOGRAPHY SYSTEM
Applicant
Diagnostic Technology, Inc.
Decision
Substantially Equivalent
Date received
1982-03-30
Decision date
1982-04-21
Days to decision
22 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Bedford, MA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.