Timentin 85MCG Sensitivity Disc
FDA 510(k) K852423 · Difco Laboratories, Inc.
510(k) numberK852423
Submission
- Device name
- Timentin 85MCG Sensitivity Disc
- Applicant
- Difco Laboratories, Inc.
Detroit, MI, US - Received
- June 7, 1985
- Decision date
- July 16, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Timentin 85MCG Sensitivity Disc cleared by the FDA?
Timentin 85MCG Sensitivity Disc (K852423) received a 510(k) decision of Substantially Equivalent on July 16, 1985, 39 days after the submission was received.