Class Class II

Aesculap AICON Container (K214041)

K214041 2022-12-30 Traditional
Home/ Devices/ Aesculap AICON Container (K214041)

Description

Aesculap AICON Container by Aesculap, Inc. — FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK214041
Clearance Date2022-12-30
Clearance TypeTraditional
Product CodeKCT
Regulation Number880.6850

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top