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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K172149FILASILK - Natural Non-absorbable Silk Surgical Suture, FILAMIDE - Non Absorbable polyamide surgical Sutures, MERICRON XL - Non Absorbable Polyester Surgical Suture, FILAPROP - Non Absorbable Polypropylene surgical Suture
K172659MEGASORB - Natural absorbable Polyglycolic Acid Surgical Suture, MITSU - Absorbable Polyglactin 910 Surgical Sutures, MITSU FST - Absorbable Polyglactin 910 Surgical Suture, FILAXYN - Absorbable Polydioxanone Surgical (PDS), FILAPRON - Absorbable poly(glycolide-co-caprolactone) Surgical Suture
K172146MERISTEEL
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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.