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ABM ANESTHESIA & BRAIN MONITOR

FDA 510(k) clearance K840232 · decided 1984-04-06

Clearance details

K-number
K840232
Device name
ABM ANESTHESIA & BRAIN MONITOR
Applicant
Datex Division Instrumentarium Corp.
Decision
Substantially Equivalent
Date received
1984-01-10
Decision date
1984-04-06
Days to decision
87 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Helsinki 10 Finland, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.