Posterior Nasal Epistaxis Instruments
FDA 510(k) K911756 · Richard Wolf Medical Instruments Corp.
510(k) numberK911756
Submission
- Device name
- Posterior Nasal Epistaxis Instruments
- Applicant
- Richard Wolf Medical Instruments Corp.
Rosemont, IL, US - Received
- April 18, 1991
- Decision date
- October 24, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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Questions and answers
When was Posterior Nasal Epistaxis Instruments cleared by the FDA?
Posterior Nasal Epistaxis Instruments (K911756) received a 510(k) decision of Substantially Equivalent on October 24, 1991, 189 days after the submission was received.
What is the product code of K911756?
The FDA product code is ECB – Unit, Syringe, Air And/Or Water, a Class I (low risk) device regulated under 21 CFR 872.4565.