Fluoro-Cep
FDA 510(k) K821060 · Zeus Scientific, Inc.
510(k) numberK821060
Submission
- Device name
- Fluoro-Cep
- Applicant
- Zeus Scientific, Inc.
Mchenry, IL, US - Received
- April 15, 1982
- Decision date
- June 22, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Fluoro-Cep cleared by the FDA?
Fluoro-Cep (K821060) received a 510(k) decision of Substantially Equivalent on June 22, 1982, 68 days after the submission was received.