Atlas FDA

UTERINE MANIPULATOR 4.5MM

FDA 510(k) clearance K841681 · decided 1984-04-23

Clearance details

K-number
K841681
Device name
UTERINE MANIPULATOR 4.5MM
Applicant
Humi Corp.
Decision
Unknown
Date received
1984-04-23
Decision date
1984-04-23
Days to decision
0 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Walker, MI, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.