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FDA 510(k)

Meriglu Topical Skin Adhesive

K-Number: K230981 · 2024-03-16

Decision Date2024-03-16
Product CodeMPN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Meriglu Topical Skin Adhesive is a medical device manufactured by M/s. Meril Endo Surgery Private Limited.. It received FDA 510(k) clearance on 2024-03-16 under approval number K230981. The device is classified under product code MPN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Meriglu Topical Skin Adhesive?

Meriglu Topical Skin Adhesive is a medical device that received FDA 510(k) clearance on 2024-03-16. It is manufactured by M/s. Meril Endo Surgery Private Limited.. The 510(k) number is K230981.

When was Meriglu Topical Skin Adhesive approved by the FDA?

Meriglu Topical Skin Adhesive received FDA 510(k) clearance on 2024-03-16, under approval number K230981.

What company makes Meriglu Topical Skin Adhesive?

Meriglu Topical Skin Adhesive is manufactured by M/s. Meril Endo Surgery Private Limited..

What is the FDA product code for Meriglu Topical Skin Adhesive?

The FDA product code for Meriglu Topical Skin Adhesive is MPN.

Other Devices by M/s. Meril Endo Surgery Private Limited.

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Related Devices (Code: MPN)

Official Source

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