Flexible Cutting Scissors
FDA 510(k) K760715 · V. Mueller O.V. Baxter Healthcare Corp.
510(k) numberK760715
Submission
- Device name
- Flexible Cutting Scissors
- Applicant
- V. Mueller O.V. Baxter Healthcare Corp.
Mchenry, IL, US - Received
- September 25, 1976
- Decision date
- October 21, 1976
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KOA – Surgical Instruments, G-U, Manual (And Accessories)
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 876.4730
- Specialty
- Gastroenterology, Urology
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Questions and answers
When was Flexible Cutting Scissors cleared by the FDA?
Flexible Cutting Scissors (K760715) received a 510(k) decision of Substantially Equivalent on October 21, 1976, 26 days after the submission was received.
What is the product code of K760715?
The FDA product code is KOA – Surgical Instruments, G-U, Manual (And Accessories), a Class I (low risk) device regulated under 21 CFR 876.4730.