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FDA 510(k)

AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G

K-Number: K232072 · 2024-02-09

ApplicantH.S Hospital Service S.P.A
Decision Date2024-02-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G is a medical device manufactured by H.S Hospital Service S.P.A. It received FDA 510(k) clearance on 2024-02-09 under approval number K232072. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G?

AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G is a medical device that received FDA 510(k) clearance on 2024-02-09. It is manufactured by H.S Hospital Service S.P.A. The 510(k) number is K232072.

When was AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G approved by the FDA?

AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G received FDA 510(k) clearance on 2024-02-09, under approval number K232072.

What company makes AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G?

AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G is manufactured by H.S Hospital Service S.P.A.

What is the FDA product code for AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G?

The FDA product code for AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G is GEI.

Other Devices by H.S Hospital Service S.P.A

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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