Quantrols Im
FDA 510(k) K771941 · Organon, Inc.
510(k) numberK771941
Submission
- Device name
- Quantrols Im
- Applicant
- Organon, Inc.
Mchenry, IL, US - Received
- October 17, 1977
- Decision date
- November 2, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Quantrols Im cleared by the FDA?
Quantrols Im (K771941) received a 510(k) decision of Substantially Equivalent on November 2, 1977, 16 days after the submission was received.