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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 the device name listed in this FDA 510(k) record. The listed applicant is Micromedics, Inc.. It received FDA 510(k) clearance on 2024-07-15 under 510(k) 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. The listed applicant is Micromedics, Inc.. The 510(k) number is K241739.

When did Endoscopic Applicator, 41 cm receive FDA 510(k) clearance?

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

Who is the listed applicant for Endoscopic Applicator, 41 cm?

The FDA 510(k) record lists Micromedics, Inc. as the applicant. This does not by itself establish the device manufacturer.

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)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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