Atlas FDA

VFI/VFE SYSTEM II

FDA 510(k) clearance K854872 · decided 1986-02-13

Clearance details

K-number
K854872
Device name
VFI/VFE SYSTEM II
Applicant
Mira, Inc.
Decision
Substantially Equivalent
Date received
1985-12-04
Decision date
1986-02-13
Days to decision
71 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Waltham, MA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.