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FDA 510(k)

MOLLI

K-Number: K210600 · 2021-04-16

ApplicantMolli Surgical, Inc.
Decision Date2021-04-16
Product CodeNEU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MOLLI is a medical device manufactured by Molli Surgical, Inc.. It received FDA 510(k) clearance on 2021-04-16 under approval number K210600. The device is classified under product code NEU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOLLI?

MOLLI is a medical device that received FDA 510(k) clearance on 2021-04-16. It is manufactured by Molli Surgical, Inc.. The 510(k) number is K210600.

When was MOLLI approved by the FDA?

MOLLI received FDA 510(k) clearance on 2021-04-16, under approval number K210600.

What company makes MOLLI?

MOLLI is manufactured by Molli Surgical, Inc..

What is the FDA product code for MOLLI?

The FDA product code for MOLLI is NEU.

Other Devices by Molli Surgical, Inc.

K231579MOLLI 2 K223107MOLLI 2 K234149MOLLI 2 System K240042MOLLI 2 System

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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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