Atlas FDA

QUANTROLS IM

FDA 510(k) clearance K771941 · decided 1977-11-02

Clearance details

K-number
K771941
Device name
QUANTROLS IM
Applicant
Organon, Inc.
Decision
Substantially Equivalent
Date received
1977-10-17
Decision date
1977-11-02
Days to decision
16 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
GONOSTICON DRI-DOT TEST (N17985/S002)Organon, Inc.1983-01-04
GONOSTICON DRI-DOT (N17985/S001)Organon, Inc.1981-04-14