Class Class II

Instylla Delivery Kit (K253769)

K253769 2025-12-22 Special
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Description

Instylla Delivery Kit by Instylla, Inc., an FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253769
Clearance Date2025-12-22
Clearance TypeSpecial
Product CodeFMF
Regulation Number880.5860

Categories

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