Atlas FDA

SCANNER TYPE 1846

FDA 510(k) clearance K827380 · decided 1982-07-09

Clearance details

K-number
K827380
Device name
SCANNER TYPE 1846
Applicant
Bruel & Kjaer Instruments, Inc.
Decision
Substantially Equivalent
Date received
1982-04-20
Decision date
1982-07-09
Days to decision
80 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Marlborough, MA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.