Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Endoscopic Applicator, 41 cm

K-Number: K241739 · 2024-07-15

ApplicantMicromedics, Inc.
Decision Date2024-07-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Endoscopic Applicator, 41 cm is a medical device manufactured by Micromedics, Inc.. It received FDA 510(k) clearance on 2024-07-15 under approval number K241739. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Endoscopic Applicator, 41 cm?

Endoscopic Applicator, 41 cm is a medical device that received FDA 510(k) clearance on 2024-07-15. It is manufactured by Micromedics, Inc.. The 510(k) number is K241739.

When was Endoscopic Applicator, 41 cm approved by the FDA?

Endoscopic Applicator, 41 cm received FDA 510(k) clearance on 2024-07-15, under approval number K241739.

What company makes Endoscopic Applicator, 41 cm?

Endoscopic Applicator, 41 cm is manufactured by Micromedics, Inc..

What is the FDA product code for Endoscopic Applicator, 41 cm?

The FDA product code for Endoscopic Applicator, 41 cm is GCJ.

Related Devices (Code: GCJ)

K163102ReliaCatch Specimen Retrieval Bag 10mm; ReliaCatch Specimen Retrieval Bag 12mmCovidien K160801Well Lead Extraction BagWell Lead Medical Co., Ltd. K153773Disposal Lens Cleaning SheathOlympus Medical Systems Corp. K161720Standard ClampStandard Bariatrics K162445LiVac Retractor SystemLivac Pty, Ltd. K162584VersaOne Bladeless TrocarCovidien

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.

↑