PYE · Class I · 21 CFR 878.4760

FDA Product Code PYE: Staple Removal Kit

This Product Code Has Been Established In Accordance With The May 20, 1997, Guidance Entitled, Convenience Kits Interim Regulatory Guidance, Found At Http://www.fda.gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm080217.pdf. This Type Of Convenience Kit, As Listed In The Guidance Above, Is Under Enforcement Discretion, And Does Not Require A Premarket Notification (510(k)) To Market If It Meets All Criteria In The Guidance.

1
Total
1
Cleared
27d
Avg days
1984
Since

FDA 510(k) Cleared Staple Removal Kit Devices (Product Code PYE)

1 devices
1–1 of 1
No devices found for this product code.

About Product Code PYE - Regulatory Context